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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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| Gepubliceerd in: | BMC Med Genet |
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| Hoofdauteurs: | , , , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
BioMed Central
2020
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7268385/ https://ncbi.nlm.nih.gov/pubmed/32487029 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12881-020-01056-4 |
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