A novel missense mutation in GJB2, p.Tyr65His, causes severe Vohwinkel syndrome.
de Zwart-Storm EA; van Geel M; Veysey E; Burge S; Cooper S; Steijlen PM; Martin PE; van Steensel MA; The British Journal Of Dermatology, 2011, vol. 164, issue 1, p 197, ISSN 13652133. ISBN 13652133.

Full Text Resources Located for this Citation

View article on EBSCOhost(Login required)
View article via CrossRef