Literature DB >> 20586835

A novel complex insertion-deletion mutation in ADAR1 gene in a Chinese family with dyschromatosis symmetrica hereditaria.

M Li, C Jin, L Yang, M Lai, Z Yao.   

Abstract

Entities:  

Mesh:

Year:  2010        PMID: 20586835     DOI: 10.1111/j.1468-3083.2010.03773.x

Source DB:  PubMed          Journal:  J Eur Acad Dermatol Venereol        ISSN: 0926-9959            Impact factor:   6.166


× No keyword cloud information.
  3 in total

1.  Five novel mutations in the ADAR1 gene associated with dyschromatosis symmetrica hereditaria.

Authors:  Qi Liu; Zhen Wang; Yuhong Wu; Lihua Cao; Qingzhu Tang; Xuesha Xing; Hongwei Ma; Shifa Zhang; Yang Luo
Journal:  BMC Med Genet       Date:  2014-06-20       Impact factor: 2.103

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

Authors:  Guolong Zhang; Minhua Shao; Zhixiu Li; Yong Gu; Xufeng Du; Xiuli Wang; Ming Li
Journal:  BMC Med Genet       Date:  2016-02-18       Impact factor: 2.103

Review 3.  Clinical and Genetic Review of Hereditary Acral Reticulate Pigmentary Disorders.

Authors:  H Alshaikh; F Alsaif; S Aldukhi
Journal:  Dermatol Res Pract       Date:  2017-10-23
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.