Identification of ATP2C1 mutations in the patients of Hailey-Hailey disease

Identification of ATP2C1 mutations in the patients of Hailey-Hailey disease

Abstract Background Familial benign chronic pemphigus, also known as Hailey-Hailey disease (HHD), is a clinically rare bullous Dermatosis. However the mechanism has not been clarified. The study aim to detect novel mutations in exons of ATP2C1 gene in HHD patients; to explore the possible mechnism o...

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Bibliographic Details
Main Authors: Xiaoli Li, Dingwei Zhang, Jiahui Ding, Li Li, Zhenghui Wang
Format: Article
Language:English
Published: BMC 2020-06-01
Series:BMC Medical Genetics
Subjects:
Familial benign chronic pemphigus
ATP2C1
Gene mutation
p63
Online Access:http://link.springer.com/article/10.1186/s12881-020-01056-4

Internet

http://link.springer.com/article/10.1186/s12881-020-01056-4

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