Four novel ADAR1 gene mutations in patients with dyschromatosis symmetrica hereditaria-Reference-Cited by-同舟云学术

Four novel ADAR1 gene mutations in patients with dyschromatosis symmetrica hereditaria

Published:2011-10-02 Issue:9 Volume:39 Page:819-821
ISSN:0385-2407
Container-title:The Journal of Dermatology
language:en
Short-container-title:

Author:

KONO Michihiro,AKIYAMA Masashi,KONDO Taisuke,SUZUKI Tamio,SUGANUMA Mutsumi,WATAYA-KANEDA Mari,LAM Joseph,SHIBAKI Akihiko,TOMITA Yasushi

Publisher

Wiley

Subject

Dermatology,General Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1346-8138.2011.01385.x/fullpdf

Reference9 articles.

1. Exclusion of linkage between dyschromatosis symmetrica hereditaria and chromosome 9;Kono;J Dermatol Sci,2000

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

3. An unwinding activity that covalently modifies its double-stranded RNA substrate;Bass;Cell,1988

4. Mutations of the KIT (mast/stem cell growth factor receptor) proto-oncogene account for a continuous range of phenotypes in human piebaldism;Spritz;Am J Hum Genet,1992

5. Mutation analysis of the ADAR1 gene in dyschromatosis symmetrica hereditaria and genetic differentiation from both dyschromatosis universalis hereditaria and acropigmentatio reticularis;Suzuki;J Invest Dermatol,2005

Cited by 4 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. Identification of five novel variants of ADAR1 in dyschromatosis symmetrica hereditaria by next-generation sequencing;Frontiers in Pediatrics;2023-07-05

2. A novel splice site mutation in theADARgene leading to exon skipping and dyschromatosis symmetrica hereditaria in a Japanese patient;Clinical and Experimental Dermatology;2016-10-16

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

4. NovelADAR1mutations including a single amino acid deletion in the deaminase domain underlie dyschromatosis symmetrica hereditaria in Japanese families;International Journal of Dermatology;2013-04-28