Autosomal Dominant Monilethrix With Incomplete Penetrance Due to a Novel KRT86 Mutation in a Chinese Family

    April 2024 in “ Anais Brasileiros de Dermatologia ”
    Ru Dai, Tingting Wang, Xianjie Wu
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    Research cited in this study 5

    1. Autosomal Recessive Monilethrix: Novel Variants of the DSG4 Gene in Three Chinese Families Molecular genetics & genomic medicine · 2022
    2. A Novel Monilethrix Mutation in Coil 2A of KRT86 Causing Autosomal Dominant Monilethrix with Incomplete Penetrance British Journal of Dermatology · 2012
    3. Congenital Hair Loss Disorders: Rare, But Not Too Rare The Journal of Dermatology · 2011
    4. De Novo Mutations in Monilethrix Experimental Dermatology · 2003
    5. Mutations in the Hair Cortex Keratin HHB6 Cause the Inherited Hair Disease Monilethrix Nature Genetics · 1997

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    1. Autosomal Dominant Monilethrix With Incomplete Penetrance Due to a Novel KRT86 Mutation in a Chinese Family Anais Brasileiros de Dermatologia · 2024