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

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 of HHD pa...

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Detalles Bibliográficos
Autores principales: Li, Xiaoli, Zhang, Dingwei, Ding, Jiahui, Li, Li, Wang, Zhenghui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7268385/
https://www.ncbi.nlm.nih.gov/pubmed/32487029
http://dx.doi.org/10.1186/s12881-020-01056-4

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7268385/
https://www.ncbi.nlm.nih.gov/pubmed/32487029
http://dx.doi.org/10.1186/s12881-020-01056-4

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