A mutation in the type II hair keratin KRT86 gene in a Han family with monilethrix()

Monilethrix, a congenital disease of hair, is usually associated with mutations in keratin genes, like KRT81, KRT83 and KRT86. We conducted this study to investigate the mutation of type II human basic hair keratin hHb/KRT gene in a Han family with monilethrix and obtain information for potential pa...

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Detalles Bibliográficos
Autores principales: Wu, Jin, Lin, Yongli, Xu, Wenrong, Li, Zhongming, Fan, Weixin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Editorial Department of Journal of Biomedical Research 2011
Materias:
Research Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3596676/
https://www.ncbi.nlm.nih.gov/pubmed/23554671
http://dx.doi.org/10.1016/S1674-8301(11)60006-7

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3596676/
https://www.ncbi.nlm.nih.gov/pubmed/23554671
http://dx.doi.org/10.1016/S1674-8301(11)60006-7

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