A missense mutation in connexin26, D66H, causes mutilating keratoderma with sensorineural deafness (Vohwinkel's syndrome) in three unrelated families (Q33864995)
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(P31) (Q13442814)
(P50) (Q4773127)
(Q37840231)
(P304) 1237-1243
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(P433) 7
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(P577) Thursday, July 1, 1999
(P921) (Q7939442)
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(P1476) "A missense mutation in connexin26, D66H, causes mutilating keratoderma with sensorineural deafness (Vohwinkel's syndrome) in three unrelated families" (language: en)
(P2093) E Maestrini
B P Korge
J Ocaña-Sierra
E Calzolari
S Cambiaghi
P M Scudder
C S Munro
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