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Article

Novel keratin 16 mutation in a Chinese family with focal palmoplantar keratoderma.

International journal of dermatology - 1 May 2021

Zhang Yuanyuan, Wu Yingda, Jia Weixue, Li Wenrui, Cheng Ping, Bu Wenbo, Li Chengrang

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Identifiers

PMID: 33377179
DOI: 10.1111/ijd.15386

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Novel keratin 16 mutation in a Chinese family with focal palmoplantar keratoderma.PMID 33377179Read ↗

A novel frameshift mutation in keratin 16 underlies pachyonychia congenita with focal palmoplantar keratoderma.Semantic proximity Read ↗

Novel mutations in keratin 16 gene underly focal non-epidermolytic palmoplantar keratoderma (NEPPK) in two familiesSemantic proximity Read ↗

A mutation in the V1 domain of K16 is responsible for unilateral palmoplantar verrucous nevus.Semantic proximity Read ↗

Keratin K6c mutations cause focal palmoplantar keratoderma.Semantic proximity Read ↗

[Keratin k6c mutations in focal palmoplantar keratoderma].Semantic proximity Read ↗

Mutation p.Leu128Pro in the 1A domain of K16 causes pachyonychia congenita with focal palmoplantar keratoderma in a Chinese family.Semantic proximity Read ↗

Novel keratin 16 mutations and protein expression studies in pachyonychia congenita type 1 and focal palmoplantar keratoderma.Semantic proximity Read ↗

Two novel de novo mutations of KRT6A and KRT16 genes in two Chinese pachyonychia congenita pedigrees with fissured tongue or diffuse plantar keratoderma.Semantic proximity Read ↗

Focal palmoplantar keratoderma in a patient with the KRT6B mutation.Semantic proximity Read ↗

Diffuse and focal palmoplantar keratoderma can be caused by a keratin 6c mutation.Semantic proximity Read ↗

Novel and recurrent keratin 6A (KRT6A) mutations in Chinese patients with pachyonychia congenita type 1.Semantic proximity Read ↗

De novo mutation of keratin 9 gene in two Taiwanese patients with epidermolytic palmoplantar keratoderma.Semantic proximity Read ↗

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