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.
Search
forLearn
0 / 0 results — no results
Research
5 / 387 results research 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 causes monilethrix in a Han family.
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.
research Pitfalls of Mapping a Large Turkish Consanguineous Family With Vertical Monilethrix Inheritance
A mutation in the KRT86 gene causes hair fragility in a Turkish family.
Community Join
0 / 0 results — no results