Literature DB >> 25189252

A novel deletion mutation of the ADAR1 gene in a Chinese patient with dyschromatosis symmetrica hereditaria.

Wei-Wei Li1, Qiu-Yue Wu, Na Li, De-Quan Deng, Ru-Song Zhang, Ying-Xia Cui, Xiao-Jun Li, Xin-Yi Xia.   

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Year:  2014        PMID： 25189252     DOI： 10.1007/s12041-014-0392-x

Source DB:  PubMed          Journal:  J Genet        ISSN： 0022-1333            Impact factor:   1.166


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  5 in total

Review 1.  Dyschromatosis symmetrica hereditaria.

Authors:  Masahiro Hayashi; Tamio Suzuki
Journal:  J Dermatol       Date:  2012-09-14       Impact factor: 4.005

Review 2.  Dyschromatosis symmetrica hereditaria (reticulate acropigmentation of Dohi): report of a Japanese family with the condition and a literature review of 185 cases.

Authors:  M Oyama; H Shimizu; Y Ohata; S Tajima; T Nishikawa
Journal:  Br J Dermatol       Date:  1999-03       Impact factor: 9.302

3.  Two novel mutations and evidence for haploinsufficiency of the ADAR gene in dyschromatosis symmetrica hereditaria.

Authors:  Q Liu; L Jiang; W-L Liu; X-J Kang; Y Ao; M Sun; Y Luo; Y Song; W H Y Lo; X Zhang
Journal:  Br J Dermatol       Date:  2006-04       Impact factor: 9.302

4.  Mutations of the RNA-specific adenosine deaminase gene (DSRAD) are involved in dyschromatosis symmetrica hereditaria.

Authors:  Yoshinori Miyamura; Tamio Suzuki; Michihiro Kono; Katsuhiko Inagaki; Shiro Ito; Noriyuki Suzuki; Yasushi Tomita
Journal:  Am J Hum Genet       Date:  2003-08-11       Impact factor: 11.025

5.  Stress-induced apoptosis associated with null mutation of ADAR1 RNA editing deaminase gene.

Authors:  Qingde Wang; Mana Miyakoda; Weidong Yang; Jaspal Khillan; David L Stachura; Mitchell J Weiss; Kazuko Nishikura
Journal:  J Biol Chem       Date:  2003-11-12       Impact factor: 5.157
  5 in total

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