A carregar...
Analysis of KRT5 and KRT14 gene mutations and mode of inheritance in Iranian patients with clinical suspicion of Epidermolysis bullosa simplex
Background: Epidermolysis bullosa simplex is a hereditary skin disorder caused by mutations in several genes such as KRT5 and KRT14 . Skin fragility in basal keratinocytes presence regions led to the cytolysis of epidermis and blistering. Aim of this study was to detect the molecular defects in KRT5...
Na minha lista:
| Publicado no: | Med J Islam Repub Iran |
|---|---|
| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Iran University of Medical Sciences
2020
|
| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7456439/ https://ncbi.nlm.nih.gov/pubmed/32884918 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.34171/mjiri.34.43 |
| Tags: |
Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!
|