research A Novel Monilethrix Mutation in Coil 2A of KRT86 Causing Autosomal Dominant Monilethrix with Incomplete Penetrance
A new mutation in the KRT86 gene causes a hair disorder with variable expression.
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5 / 413 resultsresearch Mutation Detection of Type II Hair Cortex Keratin Gene KRT86 in a Chinese Han Family With Congenital Monilethrix
A specific gene mutation in KRT86 is linked to hair disorder in a Chinese Han family.
research A Mutation in the Type II Hair Keratin KRT86 Gene in a Han Family with Monilethrix
A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.
research A mutation in the type II hair keratin KRT86 gene in a Han family with monilethrix
research Novel KRT83 and KRT86 Mutations Associated with Monilethrix
New mutations in KRT83 and KRT86 are linked to the hair disorder monilethrix.
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