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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Autori principali:	Yichuan GAN, Sanquan ZHANG, Xiaodong LI, Rujun XUE, Yidan FU, Biaoyi LUO, Wei LI
Natura:	Artigo
Lingua:	Chinês
Pubblicazione:	editoiral office of Journal of Diagnosis and Therapy on Dermato-venereology 2022-12-01
Serie:	Pifu-xingbing zhenliaoxue zazhi
Soggetti:	congenital bullous ichthyosiform erythroderma krt10 gene mutation
Accesso online:	http://pfxbzlx.gdvdc.com/CN/10.3969/j.issn.1674-8468.2022.06.007
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