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 |
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BMC,
2020-06-01T00:00:00Z.
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Internet
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A1234.567 |
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Copy 1 | Available |