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The double‐RNA‐specific adenosine deaminase (DSRAD) gene in dyschromatosis symmetrica hereditaria patients: two novel mutations and one previously described
Author(s) -
Sun XK.,
Xu AE.,
Chen JF.,
Tang X.
Publication year - 2005
Publication title -
british journal of dermatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.304
H-Index - 179
eISSN - 1365-2133
pISSN - 0007-0963
DOI - 10.1111/j.1365-2133.2005.06572.x
Subject(s) - frameshift mutation , missense mutation , genodermatosis , exon , genetics , adenosine deaminase , gene , mutation , intron , biology , microbiology and biotechnology , enzyme , biochemistry
Summary Background Dyschromatosis symmetrica hereditaria (DSH, MIM 127400) is an autosomal dominant pigmentary genodermatosis. Pathogenic mutations in the double‐RNA‐specific adenosine deaminase ( DSRAD ) gene encoding an RNA editing enzyme have recently been identified. Objectives To identify gene mutations of DSRAD in Chinese patients with DSH. Methods Three unrelated Chinese patients with DSH were subjected to mutation detection in DSRAD . Two had family histories of DSH. All the coding exons and their flanking sequences were amplified and sequenced. Results All three patients had heterozygous mutations including one non‐sense, one frameshift and one missense mutation in DSRAD. Conclusions Two novel mutations, c.3169delC (p.L1057fs) and c.3247C→T (p.R1083C), and one recurrent mutation c.1420C→T (p.R474X), were found in this series of Chinese patients with DSH.