A severe case of pachyonychia congenita type I due to a novel proline mutation in keratin 6a.

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Garcia-Rio I, Penas PF, Garcia-Diez A, McLean WH, Smith FJ

A severe case of pachyonychia congenita type I due to a novel proline mutation in keratin 6a.

Br J Dermatol. 2005 Apr;152(4):800-2.

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15840119 [ View in PubMed
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Polypeptides
NameUniProt ID
Keratin, type II cytoskeletal 6AP02538Details