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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Bibliografische Detailangaben

Hauptverfasser:	Xiaoying Ning, Shengxiang Xiao, Yanfei Zhang
Format:	Artigo
Sprache:	Inglês
Veröffentlicht:	Wolters Kluwer Medknow Publications 2022-01-01
Schriftenreihe:	Indian Journal of Dermatology
Schlagworte:	adar1 gene dyschromatosis symmetrica hereditaria genodermatose
Online-Zugang:	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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