Missense mutations in keratin 17 cause either pachyonychia congenita type 2 or a phenotype resembling steatocystoma multiplex (Q34414370)
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Language:
(P31) (Q13442814)
(P304) 220-223
(P407) (Q1860)
(P433) 2
(P478) 108
(P577) Saturday, February 1, 1997
(P921) (Q3360152)
(Q104053)
(P1433) (Q3186921)
(P1476) "Missense mutations in keratin 17 cause either pachyonychia congenita type 2 or a phenotype resembling steatocystoma multiplex" (language: en)
(P2093) Smith FJ
Corden LD
Rugg EL
Ratnavel R
Leigh IM
Moss C
Tidman MJ
Hohl D
Huber M
Kunkeler L
Munro CS
Lane EB
McLean WH
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