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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| Main Authors: | , , , , |
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| Format: | Book |
| Published: |
BMC,
2020-06-01T00:00:00Z.
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| Online Access: | Connect to this object online. |
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