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Article

Pachyonychia congenita type 2: keratin 17 mutation in a Japanese case.

Journal of the American Academy of Dermatology - 1 Jun 1998

Fujimoto W, Nakanishi G, Hirakawa S, Nakanishi T, Shimo T, Takigawa M, Arata J

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PMID: 9632020
DOI: 10.1016/s0190-9622(98)70170-7

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Related research

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Pachyonychia congenita type 2: keratin 17 mutation in a Japanese case.PMID 9632020Read ↗

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

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

Pachyonychia congenita type 2, N92S mutation of keratin 17 gene: clinical features, mutation analysis and pathological view.Semantic proximity Read ↗

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

Keratin 17 mutation in pachyonychia congenita type 2 patient with early onset steatocystoma multiplex and Hutchinson-like tooth deformity.Semantic proximity Read ↗

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

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

Mutation report: identification of a germline mutation in keratin 17 in a family with pachyonychia congenita type 2.Semantic proximity Read ↗

The genetic basis of pachyonychia congenita.Semantic proximity Read ↗

Mutation of a type II keratin gene (K6a) in pachyonychia congenitaSemantic proximity Read ↗

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

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

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