Seven novel mutations of ADAR in multi‐ethnic pedigrees with dyschromatosis symmetrica hereditaria in China

Eight Novel Mutations of the ADAR1 Gene in Chinese Patients with Dyschromatosis Symmetrica Hereditaria

(2018) Zhuang-li Tang et al.   Genetic Testing and Molecular Biomarkers

Ultrastructural study of dyschromatosis symmetrica hereditaria with widespread pigmentary eruption

(2017) Reina Omura et al.   JOURNAL OF DERMATOLOGY

Genetic spectrum of dyschromatosis symmetrica hereditaria in Chinese patients including a novel nonstop mutation in ADAR1 gene

(2016) Guolong Zhang et al.   BMC Medical Genetics

Functions of the RNA Editing Enzyme ADAR1 and Their Relevance to Human Diseases

(2016) Chunzi Song et al.   Genes

IFN-γ signaling maintains skin pigmentation homeostasis through regulation of melanosome maturation

(2014) Vivek T. Natarajan et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

The adenosine deaminase acting on RNA 1 p150 isoform is involved in the pathogenesis of dyschromatosis symmetrica hereditaria

(2013) J.Y. Zhang et al.   BRITISH JOURNAL OF DERMATOLOGY

Dyschromatosis symmetrica hereditaria

(2012) Masahiro Hayashi et al.   JOURNAL OF DERMATOLOGY

Novel clinical and molecular findings in Chinese families with dyschromatosis symmetrica hereditaria

(2011) Suju LUO et al.   JOURNAL OF DERMATOLOGY

Interferon-γ links ultraviolet radiation to melanomagenesis in mice

(2011) M. Raza Zaidi et al.   NATURE

Dyschromatosis symmetrica hereditaria: report of a sporadic case

(2010) Javier Consigli et al.   INTERNATIONAL JOURNAL OF DERMATOLOGY

Dyschromatosis symmetrica hereditaria associated with neurological disorders

(2010) Taisuke KONDO et al.   JOURNAL OF DERMATOLOGY

Six novel mutations of the ADAR1 gene in Chinese patients with dyschromatosis symmetrica hereditaria

(2008) Furen Zhang et al.   JOURNAL OF DERMATOLOGICAL SCIENCE

Six novel mutations of theADAR1gene in patients with dyschromatosis symmetrica hereditaria: Histological observation and comparison of genotypes and clinical phenotypes

(2008) Taisuke KONDO et al.   JOURNAL OF DERMATOLOGY