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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Bibliografiske detaljer
Main Authors: Wu, Jin, Lin, Yongli, Xu, Wenrong, Li, Zhongming, Fan, Weixin
Format: Artigo
Sprog:Inglês
Udgivet: Editorial Department of Journal of Biomedical Research 2011
Fag:
Research Paper
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC3596676/
https://ncbi.nlm.nih.gov/pubmed/23554671
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/S1674-8301(11)60006-7
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