Identification of Two Novel Frameshift Mutations of the ADAR1 Gene in Two Chinese Families With Dyschromatosis Symmetrica Hereditaria

Identification of Two Novel Frameshift Mutations of the ADAR1 Gene in Two Chinese Families With Dyschromatosis Symmetrica Hereditaria

Background: Dyschromatosis symmetrica hereditaria (DSH) is a rare autosomal dominant skin disease. The mutation of the ADAR1 gene is the pathogenesis of this disorder. Aims: This study aimed to identify the mutations of the ADAR1 gene in two Chinese families with DSH. Methods and Materials: Eight pa...

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Bibliographic Details
Main Authors: Xiaoying Ning, Shengxiang Xiao, Yanfei Zhang
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2022-01-01
Series:Indian Journal of Dermatology
Subjects:
adar1 gene
dyschromatosis symmetrica hereditaria
genodermatose
Online Access:http://www.e-ijd.org/article.asp?issn=0019-5154;year=2022;volume=67;issue=4;spage=355;epage=358;aulast=Ning

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http://www.e-ijd.org/article.asp?issn=0019-5154;year=2022;volume=67;issue=4;spage=355;epage=358;aulast=Ning

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