A missense mutation in connexin26, D66H, causes mutilating...

Human Molecular Genetics 1999 / 7 Vol. 8; Iss. 7

A missense mutation in connexin26, D66H, causes mutilating keratoderma with sensorineural deafness (Vohwinkel's syndrome) in three unrelated families

Maestrini, E.
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Volume:
8
Language:
english
Journal:
Human Molecular Genetics
DOI:
10.1093/hmg/8.7.1237
Date:
July, 1999
File:
PDF, 354 KB
english, 1999
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