A missense mutation in connexin26, D66H, causes mutilating keratoderma with sensorineural deafness (Vohwinkel's syndrome) in three unrelated families
Open Access
- 1 July 1999
- journal article
- research article
- Published by Oxford University Press (OUP) in Human Molecular Genetics
- Vol. 8 (7), 1237-1243
- https://doi.org/10.1093/hmg/8.7.1237