Two frameshift mutations of the double-stranded RNA-specific adenosine deaminase gene in Chinese pedigrees with dyschromatosis symmetrica hereditaria
Author:
Publisher
Wiley
Subject
Dermatology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2133.2006.07223.x/fullpdf
Reference15 articles.
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2. Refined localization of dyschromatosis symmetrica hereditaria gene to a 9·4-cM region at 1q21-22 and a literature review of 136 cases reported in China;He;Br J Dermatol,2004
3. Identification of a locus for dyschromatosis symmetrica hereditaria at chromosome 1q11-1q21;Zhang;J Invest Dermatol,2003
4. Mutations of the RNA-specific adenosine deaminase gene (DSRAD) are involved in dyschromatosis symmetrica hereditaria;Miyamura;Am J Hum Genet,2003
5. Genomic organization and chromosomal location of the human dsRNA adenosine deaminase gene: the enzyme for glutamate-activated ion channel RNA editing;Wang;J Mol Biol,1995
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1. Mutations in the ADAR1 gene in 2 Chinese families with dyschromatosis symmetrica hereditaria;Genetics and Molecular Research;2013
2. Dyschromatosis symmetrica hereditaria;The Journal of Dermatology;2012-09-14
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4. Role of ADARs in Mouse Development;Current Topics in Microbiology and Immunology;2011
5. Mutational spectrum of the ADAR1 gene in dyschromatosis symmetrica hereditaria;Archives of Dermatological Research;2010-02-26
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