A novel nonsense mutation of ADAR1 gene in a Chinese patient with dyschromatosis symmetrica hereditaria
Author:
Affiliation:
1. Institute of Laboratory Medicine; Jinling Hospital, Nanjing University School of Medicine; Nanjing China
2. Department of Dermatology; Jinling Hospital, Nanjing University School of Medicine; Nanjing China
Publisher
Wiley
Subject
Infectious Diseases,Dermatology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/jdv.12381/fullpdf
Reference8 articles.
1. Dyschromatosis symmetrica hereditaria: a retrospective case series and literature review;Peng;Dermatologica Sinica,2012
2. Dyschromatosis symmetrica hereditaria;Hayashi;J Dermatol,2013
3. Induction of protein translation by ADAR1 within living cell nuclei is not dependent on RNA editing;Herbert;Mol Cell,2002
4. Genomic organization and chromosomal location of the human dsRNA adenosine deaminase gene: the enzyme for glutamate-activatedion channel RNA editing;Wang;J Mol Biol,1995
5. Two novel mutations and evidence for haploinsufficiency of the ADAR gene in dyschromatosis symmetrica hereditaria;Liu;Br J Dermatol,2006
Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Two novel mutations of the ADAR1 gene in Chinese patients with dyschromatosis symmetrica hereditaria successfully treated with fractional CO2 laser;Journal of the European Academy of Dermatology and Venereology;2015-03-12
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