Mutation analyses of patients with dyschromatosis symmetrica hereditaria: Five novel mutations of the ADAR1 gene-Reference-Cited by-同舟云学术

Mutation analyses of patients with dyschromatosis symmetrica hereditaria: Five novel mutations of the ADAR1 gene

Published:2010-06 Issue:3 Volume:58 Page:218-220
ISSN:0923-1811
Container-title:Journal of Dermatological Science
language:en
Short-container-title:Journal of Dermatological Science

Author:

Murata Ichidai,Hayashi Masahiro,Hozumi Yutaka,Fujii Kazuyasu,Mitsuhashi Yoshihiko,Oiso Naoki,Fukai Kazuyoshi,Kuroki Nozomi,Mori Yasuki,Utani Atsushi,Tomita Yasushi,Fujita Yasuyuki,Suzuki Tamio

Publisher

Elsevier BV

Subject

Dermatology,Molecular Biology,Biochemistry

Reference10 articles.

1. Genetics of pigmentary disorders;Tomita;Am J Med Genet C Semin Med Genet,2004

2. Mutations of the RNA-specific adenosine deaminase gene (DSRAD) are involved in dyschromatosis symmetrica hereditaria;Miyamura;Am J Hum Genet,2003

3. Six novel mutations of the ADAR1 gene in Chinese patients with dyschromatosis symmetrica hereditaria;Zhang;J Dermatol Sci,2008

4. Six novel mutations of the ADAR1 gene in patients with dyschromatosis symmetrica hereditaria: Histological observation and comparison of genotypes and clinical phenotypes;Kondo;J Dermatol,2008

5. A missense mutation c.G2747A (p.R916Q) of ADAR1 gene in dyschromatosis symmetrica hereditaria is not a novel mutation;Hayashi;Arch Dermatol Res,2010

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1. Identification of five novel variants of ADAR1 in dyschromatosis symmetrica hereditaria by next-generation sequencing;Frontiers in Pediatrics;2023-07-05

2. Dyschromatosis;Harper's Textbook of Pediatric Dermatology;2019-11-20

3. Analysis of genotype/phenotype correlations in Japanese patients with dyschromatosis symmetrica hereditaria;NAGOYA J MED SCI;2018

4. A novel missense mutation of $$\textit{ADAR1}$$ ADAR 1 gene in a Chinese family leading to dyschromatosis symmetrica hereditaria and literature review;Journal of Genetics;2017-12

5. Five novel mutations in the ADAR1 gene associated with dyschromatosis symmetrica hereditaria;BMC Medical Genetics;2014-06-20