A case report of congenital bullous ichthyosiform erythroderma caused by a mutation of KRT10 gene
Objective To identify KRT1 and KRT10 gene mutation in a patient with bullous ichthyosiform erythroderma (BCIE). Methods Peripheral bloods of the patient and her families were collected and DNAs were extracted. All coding exons and flanking sequence of the KRT1 and KRT10 genes were amplified by PCR....
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| Autors principals: | , , , , , , |
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| Format: | Artigo |
| Idioma: | Chinês |
| Publicat: |
editoiral office of Journal of Diagnosis and Therapy on Dermato-venereology
2022-12-01
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| Col·lecció: | Pifu-xingbing zhenliaoxue zazhi |
| Matèries: | |
| Accés en línia: | http://pfxbzlx.gdvdc.com/CN/10.3969/j.issn.1674-8468.2022.06.007 |
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