A novel missense mutation in GJB2, p.Tyr65His, causes severe Vohwinkel syndrome.
de Zwart-Storm, E. A.; van Geel, M.; Veysey, E.; Burge, S.; Cooper, S.; Steijlen, P. M.; Martin, P. E.; van Steensel, M. A. M.; British Journal of Dermatology, 2011, vol. 164, issue 1, p 197, ISSN 00070963. ISBN 13652133.

Full Text Resources Located for this Citation

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