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Article

Pachyonychia congenita in Japan: report of familial cases with a recurrent KRT16 mutation.

European journal of dermatology : EJD - 1 Jan 2000

Inaba Yutaka, Kanazawa Nobuo, Furukawa Fukumi, Sakurane Yoshihisa, Nakano Hajime, Sawamura Daisuke, Yoneda Kozo, Hamada Takahiro, Hashimoto Takashi

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Identifiers

PMID: 24491404
DOI: 10.1684/ejd.2013.2244

Genes

KRT16

Provenance

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Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Pachyonychia congenita in Japan: report of familial cases with a recurrent KRT16 mutation.PMID 24491404Read ↗

A recurrent missense mutation in the KRT16 gene causing pachyonychia congenita in a patient.Semantic proximity Read ↗

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

Mutations of KRT6A are more frequent than those of KRT16 in pachyonychia congenita type 1: report of a novel and a recently reported mutation in two unrelated Chinese families.Semantic proximity Read ↗

Pachyonychia congenita type 2: keratin 17 mutation in a Japanese case.Semantic proximity Read ↗

Early severe pachyonychia congenita subtype PC-K6a with a novel mutation in the KRT6A gene.Semantic proximity Read ↗

A novel mutation in K6b in pachyonychia congenita type 2.Semantic proximity Read ↗

Recurrent mutation in keratin 17 in a large family with pachyonychia congenita type 2.Semantic proximity Read ↗

A novel KRT6A mutation in a case of pachyonychia congenita from India.Semantic proximity Read ↗

[Keratin 17 mutation in pachyonychia congenita type 2 in a Chinese Han family].Semantic proximity Read ↗

[Pachyonychia congenita. Molecular genetic analysis simplifies clinical classification in subtypes].Semantic proximity Read ↗

[Pachyonychia congenita type 2 due to mutation in the keratin 6b gene].Semantic proximity Read ↗

Identification of two recurrent mutations in keratin genes in three cases with pachyonychia congenita.Semantic proximity Read ↗

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