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A novel missense mutation in GJB2, p.Tyr65His, causes severe Vohwinkel syndrome
E.A. de Zwart-Storm, M. van Geel, E. Veysey, S. Burge, S. Cooper, P.M. Steijlen, P.E. Martin, M.A.M. van SteenselVolume:
164
Année:
2011
Langue:
english
Pages:
3
DOI:
10.1111/j.1365-2133.2010.10058.x
Fichier:
PDF, 317 KB
english, 2011