A novel mutation in LPAR6 causes autosomal recessive hypotrichosis of the scalp

Mutations in Lipase H Gene Underlie Autosomal Recessive Hypotrichosis in Five Pakistani Families

(2010) Ue Kalsoom et al.   ACTA DERMATO-VENEREOLOGICA

Homozygous Mutations in the 5′ Region of the JUP Gene Result in Cutaneous Disease but Normal Heart Development in Children

(2010) Rita M. Cabral et al.   JOURNAL OF INVESTIGATIVE DERMATOLOGY

APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex

(2010) Yutaka Shimomura et al.   NATURE

A Homozygous Nonsense Mutation in the Human Desmocollin-3 (DSC3) Gene Underlies Hereditary Hypotrichosis and Recurrent Skin Vesicles

(2009) Muhammad Ayub et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Wnt Signaling, Lgr5, and Stem Cells in the Intestine and Skin

(2009) Andrea Haegebarth et al.   AMERICAN JOURNAL OF PATHOLOGY

Novel mutations in the P2RY5 gene in one Turkish and two Indian patients presenting with hypotrichosis and woolly hair

(2009) Sandra M. Pasternack et al.   ARCHIVES OF DERMATOLOGICAL RESEARCH

Novel truncating mutations inPKP1andDSPcause similar skin phenotypes in two Brazilian families

(2009) A. Tanaka et al.   BRITISH JOURNAL OF DERMATOLOGY

Mutations in theP2RY5gene underlie autosomal recessive hypotrichosis in 13 Pakistani families

(2009) M. Tariq et al.   BRITISH JOURNAL OF DERMATOLOGY

A novel deletion mutation in LIPH gene causes autosomal recessive hypotrichosis (LAH2)

(2009) M Jelani et al.   CLINICAL GENETICS

A missense mutation in the P2RY5 gene leading to autosomal recessive woolly hair in a Syrian patient

(2009) M. Kurban et al.   JOURNAL OF DERMATOLOGICAL SCIENCE

Founder Mutations in the Lipase H Gene in Families with Autosomal Recessive Woolly Hair/Hypotrichosis

(2009) Yutaka Shimomura et al.   JOURNAL OF INVESTIGATIVE DERMATOLOGY

In Vitro Analysis of LIPH Mutations Causing Hypotrichosis Simplex: Evidence Confirming the Role of Lipase H and Lysophosphatidic Acid in Hair Growth

(2009) Sandra M. Pasternack et al.   JOURNAL OF INVESTIGATIVE DERMATOLOGY

Mutations in lipase H cause autosomal recessive hypotrichosis simplex with woolly hair

(2009) Liran Horev et al.   JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY

A novel deletion mutation in P2RY5/LPA6 gene cause autosomal recessive woolly hair with hypotrichosis

(2009) L Horev et al.   JOURNAL OF THE EUROPEAN ACADEMY OF DERMATOLOGY AND VENEREOLOGY

A large duplication in LIPH underlies autosomal recessive hypotrichosis simplex in four Middle Eastern families

(2008) Sagi Nahum et al.   ARCHIVES OF DERMATOLOGICAL RESEARCH

A novel deletion mutation in the phospholipase H (LIPH) gene in a consanguineous Pakistani family with autosomal recessive hypotrichosis (LAH2)

(2008) S. Kamran-ul-Hassan Naqvi et al.   BRITISH JOURNAL OF DERMATOLOGY

Autosomal recessive woolly hair with hypotrichosis caused by a novel homozygous mutation in theP2RY5gene

(2008) Yutaka Shimomura et al.   EXPERIMENTAL DERMATOLOGY

Genome-wide linkage analysis of an autosomal recessive hypotrichosis identifies a novel P2RY5 mutation

(2008) Lynn Petukhova et al.   GENOMICS

Novel mutations in G protein-coupled receptor gene (P2RY5) in families with autosomal recessive hypotrichosis (LAH3)

(2008) Zahid Azeem et al.   HUMAN GENETICS

Mutations in the Lipase H Gene Underlie Autosomal Recessive Woolly Hair/Hypotrichosis

(2008) Yutaka Shimomura et al.   JOURNAL OF INVESTIGATIVE DERMATOLOGY

G protein–coupled receptor P2Y5 and its ligand LPA are involved in maintenance of human hair growth

(2008) Sandra M Pasternack et al.   NATURE GENETICS

Disruption of P2RY5, an orphan G protein–coupled receptor, underlies autosomal recessive woolly hair

(2008) Yutaka Shimomura et al.   NATURE GENETICS