Hermansky–Pudlak syndrome: Mutation update

Crohn’s-like acute severe colitis associated with Hermansky-Pudlak syndrome: A case report

(2019) Paul Girot et al.   WORLD JOURNAL OF GASTROENTEROLOGY

Hermansky-Pudlak syndrome and oculocutaneous albinism in Chinese children with pigmentation defects and easy bruising

(2019) Bradley Power et al.   Orphanet Journal of Rare Diseases

Familial Pulmonary Fibrosis and Hermansky-Pudlak Syndrome Rare Missense Mutations In Context

(2019) Robert S Stearman et al.   AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE

Identification of novel variants in ten patients with Hermansky-Pudlak syndrome by high-throughput sequencing

(2019) Jose María Bastida et al.   ANNALS OF MEDICINE

Identification of candidate cancer predisposing variants by performing whole-exome sequencing on index patients from BRCA1 and BRCA2-negative breast cancer families

(2019) Rajendra Bahadur Shahi et al.   BMC CANCER

Precise therapeutic gene correction by a simple nuclease-induced double-stranded break

(2019) Sukanya Iyer et al.   NATURE

NGS‐based targeted resequencing identified rare subtypes of albinism; providing accurate molecular diagnosis for Japanese patients with albinism

(2019) Ken Okamura et al.   Pigment Cell & Melanoma Research

The road to lysosome‐related organelles: Insights from Hermansky‐Pudlak syndrome and other rare diseases

(2019) Shanna L. Bowman et al.   TRAFFIC

Hermansky-Pudlak syndrome type II and lethal hemophagocytic lymphohistiocytosis: Case description and review of the literature

(2019) Fabiola Dell’Acqua et al.   Journal of Allergy and Clinical Immunology-In Practice

Modeling of Fibrotic Lung Disease Using 3D Organoids Derived from Human Pluripotent Stem Cells

(2019) Alexandros Strikoudis et al.   Cell Reports

In Vitro Disease Modeling of Hermansky-Pudlak Syndrome Type 2 Using Human Induced Pluripotent Stem Cell-Derived Alveolar Organoids

(2019) Yohei Korogi et al.   Stem Cell Reports

Treatment of Hermansky-Pudlak syndrome Associated granulomatous colitis with anti-TNF agents

(2019) Coskun Ozer Demirtas et al.   EUROPEAN JOURNAL OF GASTROENTEROLOGY & HEPATOLOGY

A novel mutation causes Hermansky-Pudlak syndrome type 4 with pulmonary fibrosis in 2 siblings from China

(2019) Wenjuan Wu et al.   MEDICINE

Subclinical hypopigmentation of the skin and hair in a Japanese patient with Hermansky–Pudlak syndrome type 3

(2019) Sonoko Saito et al.   JOURNAL OF DERMATOLOGY

Novel genetic variant of HPS1 gene in Hermansky-Pudlak syndrome with fulminant progression of pulmonary fibrosis: a case report

(2019) Martina Doubková et al.   BMC Pulmonary Medicine

Gene-edited MLE-15 Cells as a Model for the Hermansky-Pudlak Syndromes

(2018) Seunghyi Kook et al.   AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY

A novel nonsense mutation in a patient with Hermansky-Pudlak syndrome type 4

(2018) Kirstin Sandrock-Lang et al.   BLOOD CELLS MOLECULES AND DISEASES

Targeted resequencing reveals genetic risks in patients with sporadic idiopathic pulmonary fibrosis

(2018) Yanhan Deng et al.   HUMAN MUTATION

Hermansky-Pudlak syndrome type 2 manifests with fibrosing lung disease early in childhood

(2018) Meike Hengst et al.   Orphanet Journal of Rare Diseases

Molecular characterization of a series of 990 index patients with albinism

(2018) Eulalie Lasseaux et al.   Pigment Cell & Melanoma Research

Clinical management and outcomes of patients with Hermansky-Pudlak syndrome pulmonary fibrosis evaluated for lung transplantation

(2018) Souheil El-Chemaly et al.   PLoS One

Hermansky-Pudlak syndrome with a novel genetic variant inHPS1and subsequent accelerated pulmonary fibrosis: significance for phenocopy diseases

(2018) Oliver J McElvaney et al.   THORAX

Variations in Dysbindin-1 are associated with cognitive response to antipsychotic drug treatment

(2018) Diego Scheggia et al.   Nature Communications

Integrative Analyses of De Novo Mutations Provide Deeper Biological Insights into Autism Spectrum Disorder

(2018) Atsushi Takata et al.   Cell Reports

Pallidin is a novel interacting protein for cytohesin-2 and regulates the early endosomal pathway and dendritic formation in neurons

(2018) Akiko Ito et al.   JOURNAL OF NEUROCHEMISTRY

Prolonged treatment with open-label pirfenidone in Hermansky-Pudlak syndrome pulmonary fibrosis

(2018) Kevin J. O'Brien et al.   MOLECULAR GENETICS AND METABOLISM

Severe bleeding with subclinical oculocutaneous albinism in a patient with a novel HPS6 missense variant

(2018) Chen G. Han et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Biallelic mutations in AP3D1 cause Hermansky-Pudlak syndrome type 10 associated with immunodeficiency and seizure disorder

(2018) Mohammed Mohammed et al.   European Journal of Medical Genetics

Targeted high-throughput sequencing technique for the molecular diagnosis of primary immunodeficiency disorders

(2018) Zuo Hua Chi et al.   MEDICINE

Predictable and precise template-free CRISPR editing of pathogenic variants

(2018) Max W. Shen et al.   NATURE

Instability of BLOC-2 and BLOC-3 in Chinese Patients with Hermansky-Pudlak Syndrome

(2018) Aihua Wei et al.   Pigment Cell & Melanoma Research

Hermansky-Pudlak syndrome type 2: Aberrant pre-mRNA splicing and mislocalization of granule proteins in neutrophils

(2017) Martin de Boer et al.   HUMAN MUTATION

Exome sequencing for simultaneous mutation screening in children with hemophagocytic lymphohistiocytosis

(2017) Ekchol Mukda et al.   INTERNATIONAL JOURNAL OF HEMATOLOGY

Dysbindin-1 Involvement in the Etiology of Schizophrenia

(2017) Haitao Wang et al.   INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES

Effective Immunological Guidance of Genetic Analyses Including Exome Sequencing in Patients Evaluated for Hemophagocytic Lymphohistiocytosis

(2017) Sandra Ammann et al.   JOURNAL OF CLINICAL IMMUNOLOGY

The curse of idiopathic

(2017) Kevin J. O’Brien et al.   JOURNAL OF INHERITED METABOLIC DISEASE

Clinical and molecular phenotyping of a child with Hermansky-Pudlak syndrome-7, an uncommon genetic type of HPS

(2017) Melanie M. Bryan et al.   MOLECULAR GENETICS AND METABOLISM

ClinVar: improving access to variant interpretations and supporting evidence

(2017) Melissa J Landrum et al.   NUCLEIC ACIDS RESEARCH

Characterization of melanosomes and melanin in Japanese patients with Hermansky-Pudlak syndrome types 1, 4, 6, and 9

(2017) Ken Okamura et al.   Pigment Cell & Melanoma Research

Clinico-molecular analysis of eleven patients with Hermansky-Pudlak type 5 syndrome, a mild form of HPS

(2017) Vincent Michaud et al.   Pigment Cell & Melanoma Research

Hermansky-Pudlak syndrome subtype 5 (HPS-5) novel mutation in a 65 year-old with oculocutaneous hypopigmentation and mild bleeding diathesis: The importance of recognizing a subtle phenotype

(2017) Juliana Perez Botero et al.   PLATELETS

Sequence-Based Mapping and Genome Editing Reveal Mutations in Stickleback Hps5 Cause Oculocutaneous Albinism and the casper Phenotype

(2017) James C. Hart et al.   G3-Genes Genomes Genetics

Increased autophagic sequestration in adaptor protein-3 deficient dendritic cells limits inflammasome activity and impairs antibacterial immunity

(2017) Adriana R. Mantegazza et al.   PLoS Pathogens

Cellular and molecular defects in a patient with Hermansky-Pudlak syndrome type 5

(2017) Joshi Stephen et al.   PLoS One

Impairment of dendritic cell functions in patients with adaptor protein-3 complex deficiency

(2016) Alberto Prandini et al.   BLOOD

Mutations in AP3D1 associated with immunodeficiency and seizures define a new type of Hermansky-Pudlak syndrome

(2016) S. Ammann et al.   BLOOD

A high-throughput sequencing test for diagnosing inherited bleeding, thrombotic, and platelet disorders

(2016) I. Simeoni et al.   BLOOD

Natural killer cell activity and dysfunction in Hermansky-Pudlak syndrome

(2016) Aleksandra Gil-Krzewska et al.   BRITISH JOURNAL OF HAEMATOLOGY

The ophthalmic presentation of Hermansky–Pudlak syndrome 6

(2016) Sarah Hull et al.   BRITISH JOURNAL OF OPHTHALMOLOGY

Hermansky-Pudlak syndrome genes are frequently mutated in patients with albinism from the Arabian Peninsula

(2016) A. O. Khan et al.   CLINICAL GENETICS

Clinical exome sequencing: results from 2819 samples reflecting 1000 families

(2016) Daniel Trujillano et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Clinical genomics can facilitate countrywide estimation of autosomal recessive disease burden

(2016) Mohamed Abouelhoda et al.   GENETICS IN MEDICINE

Increasing the sensitivity of clinical exome sequencing through improved filtration strategy

(2016) Hanan E. Shamseldin et al.   GENETICS IN MEDICINE

HGVS Recommendations for the Description of Sequence Variants: 2016 Update

(2016) Johan T. den Dunnen et al.   HUMAN MUTATION

Case of Japanese Hermansky-Pudlak syndrome patient with deeply invasive squamous cell carcinoma and multiple lesions of actinic keratosis on the face and neck

(2016) Yohei Iwata et al.   JOURNAL OF DERMATOLOGY

BLOC-2 subunit HPS6 deficiency affects the tubulation and secretion of von Willebrand factor from mouse endothelial cells

(2016) Jing Ma et al.   Journal of Genetics and Genomics

Novel HPS6 mutations identified by whole-exome sequencing in two Japanese sisters with suspected ocular albinism

(2016) Daisuke Miyamichi et al.   JOURNAL OF HUMAN GENETICS

Super-resolution microscopy as a potential approach to diagnosis of platelet granule disorders

(2016) D. Westmoreland et al.   JOURNAL OF THROMBOSIS AND HAEMOSTASIS

Identification of a novel mutation in HPS6 in a patient with hemophilia B and oculocutaneous albinism

(2016) Kevin J. O'Brien et al.   MOLECULAR GENETICS AND METABOLISM

Cutaneous freckling: Possible new clinical marker for the diagnosis of Hermansky-Pudlak syndrome in Indian Asian patients with oculocutaneous albinism

(2016) Karthikeyan Arcot Sadagopan et al.   OPHTHALMIC GENETICS

A novel two-nucleotide deletion in HPS6 affects mepacrine uptake and platelet dense granule secretion in a family with Hermansky-Pudlak syndrome

(2016) Oliver Andres et al.   PEDIATRIC BLOOD & CANCER

Clinical presentation and outcome of pediatric patients with hemophagocytic lymphohistiocytosis in China: A retrospective multicenter study

(2016) Xiao-Jun Xu et al.   PEDIATRIC BLOOD & CANCER

NGS-based 100-gene panel of hypopigmentation identifies mutations in Chinese Hermansky-Pudlak syndrome patients

(2016) Aihua Wei et al.   Pigment Cell & Melanoma Research

Causal variants screened by whole exome sequencing in a patient with maternal uniparental isodisomy of chromosome 10 and a complicated phenotype

(2016) NIU LI et al.   Experimental and Therapeutic Medicine

Diagnostics of Primary Immunodeficiencies through Next-Generation Sequencing

(2016) Vera Gallo et al.   Frontiers in Immunology

Immunophenotypic and Ultrastructural Analysis of Mast Cells in Hermansky-Pudlak Syndrome Type-1: A Possible Connection to Pulmonary Fibrosis

(2016) Arnold S. Kirshenbaum et al.   PLoS One

BORC, a Multisubunit Complex that Regulates Lysosome Positioning

(2015) Jing Pu et al.   DEVELOPMENTAL CELL

Recognition deficits in mice carrying mutations of genes encoding BLOC-1 subunits pallidin or dysbindin

(2015) S. Spiegel et al.   GENES BRAIN AND BEHAVIOR

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology

(2015) Sue Richards et al.   GENETICS IN MEDICINE

Synergistic defects of UNC13D and AP3B1 leading to adult hemophagocytic lymphohistiocytosis

(2015) Lili Gao et al.   INTERNATIONAL JOURNAL OF HEMATOLOGY

Patients with Griscelli syndrome and normal pigmentation identify RAB27A mutations that selectively disrupt MUNC13-4 binding

(2015) Valentina Cetica et al.   JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY

Case of Hermansky-Pudlak syndrome 1 in a Japanese infant

(2015) Mari Tanaka et al.   JOURNAL OF DERMATOLOGY

Prenatal Genotyping of Four Common Oculocutaneous Albinism Genes in 51 Chinese Families

(2015) Ai-Hua Wei et al.   Journal of Genetics and Genomics

Management of Tooth Extraction in a Patient With a Rare Bleeding Disorder Associated With Hermansky-Pudlak Syndrome: A Case Report

(2015) Patton Minkin et al.   JOURNAL OF ORAL AND MAXILLOFACIAL SURGERY

In vitro functional correction of Hermansky–Pudlak Syndrome type-1 by lentiviral-mediated gene transfer

(2015) Yasuhiro Ikawa et al.   MOLECULAR GENETICS AND METABOLISM

Identification and clinical characterization of Hermansky-Pudlak syndrome alleles in the Pakistani population

(2015) Sairah Yousaf et al.   Pigment Cell & Melanoma Research

Targeted high-throughput sequencing for genetic diagnostics of hemophagocytic lymphohistiocytosis

(2015) Bianca Tesi et al.   Genome Medicine

Hermansky-Pudlak syndrome

(2014) I. Sánchez-Guiu et al.   Hamostaseologie

An Intractable Case of Hermansky-Pudlak Syndrome

(2014) Masaki Kanazu et al.   INTERNAL MEDICINE

Hermansky-Pudlak Syndrome with Nonspecific Interstitial Pneumonia

(2014) Kazuki Furuhashi et al.   INTERNAL MEDICINE

An Autopsy Case of Hermansky-Pudlak Syndrome: A Case Report and Review of the Literature on Treatment

(2014) Tatsuhiko Harada et al.   INTERNAL MEDICINE

The unique association of iris heterochromia with Hermansky Pudlak syndrome

(2014) C. Gail Summers et al.   JOURNAL OF AAPOS

Case of Hermansky-Pudlak syndrome 1 patient with milder symptoms in Japanese

(2014) Seiji Takeuchi et al.   JOURNAL OF DERMATOLOGY

Hermansky-Pudlak syndrome type 4 with a novel mutation

(2014) Yuta Araki et al.   JOURNAL OF DERMATOLOGY

De novo mutations in schizophrenia implicate synaptic networks

(2014) Menachem Fromer et al.   NATURE

The contribution of de novo coding mutations to autism spectrum disorder

(2014) Ivan Iossifov et al.   NATURE

The risk of hemophagocytic lymphohistiocytosis in Hermansky-Pudlak syndrome type 2

(2013) B. Jessen et al.   BLOOD

Disruption of AP3B1by a chromosome 5 inversion: a new disease mechanism in Hermansky-Pudlak syndrome type 2

(2013) Matthew L Jones et al.   BMC Medical Genetics

Association of the Hermansky–Pudlak syndrome type 4 (HPS4) gene variants with cognitive function in patients with schizophrenia and healthy subjects

(2013) Go Kuratomi et al.   BMC Psychiatry

Lysosome-related organelles: unusual compartments become mainstream

(2013) Michael S Marks et al.   CURRENT OPINION IN CELL BIOLOGY

snow white, a Zebrafish Model of Hermansky-Pudlak Syndrome Type 5

(2013) C. M. S. Daly et al.   GENETICS

Hermansky-Pudlak syndrome (HPS5) in a nonagenarian

(2013) Alexander L. Ringeisen et al.   JOURNAL OF AAPOS

The unique association of iris heterochromia with Hermansky-Pudlak syndrome

(2013) Phillip Radke et al.   JOURNAL OF AAPOS

Hermansky-Pudlak Syndrome: Health Care Throughout Life

(2013) S. L. Seward et al.   PEDIATRICS

The mouse ruby-eye 2d(ru2d/Hps5ru2-d) allele inhibits eumelanin but not pheomelanin synthesis

(2013) Tomohisa Hirobe et al.   Pigment Cell & Melanoma Research

An association study of the Hermansky–Pudlak syndrome type 4 gene in schizophrenic patients

(2013) Atsushi Saito et al.   PSYCHIATRIC GENETICS

Microsatellite markers as a rapid approach for autozygosity mapping in Hermansky-Pudlak syndrome: Identification of the second HPS7 mutation in a patient presenting late in life

(2013) Gillian C. Lowe et al.   THROMBOSIS AND HAEMOSTASIS

The Hermansky-Pudlak Syndrome: Clinical Features and Imperatives from an Ophthalmic Perspective

(2013) Andrew J. Schneier et al.   Seminars in Ophthalmology

The Alveolar Epithelium Determines Susceptibility to Lung Fibrosis in Hermansky-Pudlak Syndrome

(2012) Lisa R. Young et al.   AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE

A divalent interaction between HPS1 and HPS4 is required for the formation of the biogenesis of lysosome-related organelle complex-3 (BLOC-3)

(2012) Carmelo Carmona-Rivera et al.   BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH

Exome sequencing reveals a pallidin mutation in a Hermansky-Pudlak-like primary immunodeficiency syndrome

(2012) R. Badolato et al.   BLOOD

Adaptor Protein-3 in Dendritic Cells Facilitates Phagosomal Toll-like Receptor Signaling and Antigen Presentation to CD4+ T Cells

(2012) Adriana R. Mantegazza et al.   IMMUNITY

Unknown

(2012) Bernadette Gochuico et al.   MOLECULAR MEDICINE

A BLOC-1 mutation screen reveals a novel BLOC1S3 mutation in Hermansky-Pudlak Syndrome type 8

(2012) Andrew R. Cullinane et al.   Pigment Cell & Melanoma Research

Novel mutation in Hermansky–Pudlak syndrome type 2 with mild immunological phenotype

(2012) Karin Kurnik et al.   PLATELETS

Dysbindin-Containing Complexes and their Proposed Functions in Brain: From Zero to (too) Many in a Decade

(2011) Cristina A Ghiani et al.   ASN Neuro

LOVD v.2.0: the next generation in gene variant databases

(2011) Ivo F. A. C. Fokkema et al.   HUMAN MUTATION

Implementation of an optimized strategy for genetic testing of the Chinese patients with oculocutaneous albinism

(2011) Aihua Wei et al.   JOURNAL OF DERMATOLOGICAL SCIENCE

Clinical, Molecular, and Cellular Features of Non-Puerto Rican Hermansky–Pudlak Syndrome Patients of Hispanic Descent

(2011) Carmelo Carmona-Rivera et al.   JOURNAL OF INVESTIGATIVE DERMATOLOGY

Rapid genetic diagnosis of heritable platelet function disorders with next-generation sequencing: proof-of-principle with Hermansky-Pudlak syndrome

(2011) M. L. JONES et al.   JOURNAL OF THROMBOSIS AND HAEMOSTASIS

Pirfenidone for the treatment of Hermansky–Pudlak syndrome pulmonary fibrosis

(2011) Kevin O'Brien et al.   MOLECULAR GENETICS AND METABOLISM

The bisretinoids of retinal pigment epithelium

(2011) Janet R. Sparrow et al.   PROGRESS IN RETINAL AND EYE RESEARCH

Epithelial Stress and Apoptosis Underlie Hermansky-Pudlak Syndrome–associated Interstitial Pneumonia

(2010) Poornima Mahavadi et al.   AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE

Novel mutations in the HPS1 gene among Puerto Rican patients

(2010) C Carmona-Rivera et al.   CLINICAL GENETICS

The Management of Gastrointestinal Disease in Hermansky-Pudlak Syndrome

(2010) Adrian J. Mora et al.   JOURNAL OF CLINICAL GASTROENTEROLOGY

Hermansky-Pudlak Protein Complexes, AP-3 and BLOC-1, Differentially Regulate Presynaptic Composition in the Striatum and Hippocampus

(2010) K. Newell-Litwa et al.   JOURNAL OF NEUROSCIENCE

Hermansky-Pudlak Syndrome: Severe Colitis and Good Response to Infliximab

(2010) LM Felipez et al.   JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION

Newborn Screening for Hermansky-Pudlak Syndrome Type 3 in Puerto Rico

(2010) Maribel Torres-Serrant et al.   JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY

Hermansky-Pudlak syndrome: the importance of molecular subtyping

(2010) N. THIELEN et al.   JOURNAL OF THROMBOSIS AND HAEMOSTASIS

Compound Heterozygous Mutations in 2 Siblings with Hermansky-Pudlak Syndrome Type 1 (HPS1)

(2010) K. Sandrock et al.   KLINISCHE PADIATRIE

Novel mutation causing Hermansky-Pudlak Syndrome Type 2

(2010) Pei-Wen Chiang et al.   PEDIATRIC BLOOD & CANCER

Bifurcation of Toll-Like Receptor 9 Signaling by Adaptor Protein 3

(2010) M. Sasai et al.   SCIENCE

Hermansky-Pudlak syndrome in two African-American brothers

(2009) Melissa A. Merideth et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Alveolar Macrophage Dysregulation in Hermansky-Pudlak Syndrome Type 1

(2009) Farshid N. Rouhani et al.   AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE

Neutrophil elastase–processing defect in cyclic hematopoietic dogs

(2009) Ronghua Meng et al.   EXPERIMENTAL HEMATOLOGY

Two patients with Hermansky Pudlak syndrome type 2 and novel mutations in AP3B1

(2009) M. Wenham et al.   HAEMATOLOGICA

Transposable elements in disease-associated cryptic exons

(2009) Igor Vorechovsky   HUMAN GENETICS

The first case report of a Chinese Hermansky–Pudlak syndrome patient with a novel mutation on HPS1 gene

(2009) Aihua Wei et al.   JOURNAL OF DERMATOLOGICAL SCIENCE

A Comprehensive Analysis Reveals Mutational Spectra and Common Alleles in Chinese Patients with Oculocutaneous Albinism

(2009) Aihua Wei et al.   JOURNAL OF INVESTIGATIVE DERMATOLOGY

Clinical and cellular characterisation of Hermansky-Pudlak syndrome type 6

(2009) M Huizing et al.   JOURNAL OF MEDICAL GENETICS

Hermansky–Pudlak syndrome type 1 in patients of Indian descent

(2009) Lisa M. Vincent et al.   MOLECULAR GENETICS AND METABOLISM

Association study of DTNBP1 with schizophrenia in a US sample

(2009) Lingjun Zuo et al.   PSYCHIATRIC GENETICS

Disorders of Lysosome-Related Organelle Biogenesis: Clinical and Molecular Genetics

(2008) Marjan Huizing et al.   Annual Review of Genomics and Human Genetics

A novel mutation in a Turkish patient with Hermansky–Pudlak syndrome type 5

(2008) Lindy-Anne Korswagen et al.   EUROPEAN JOURNAL OF HAEMATOLOGY

An immunoblotting assay to facilitate the molecular diagnosis of Hermansky–Pudlak syndrome

(2008) Ramin Nazarian et al.   MOLECULAR GENETICS AND METABOLISM

Early Visual Processing Deficits in Dysbindin-Associated Schizophrenia

(2007) Gary Donohoe et al.   BIOLOGICAL PSYCHIATRY