Authors:
Maestrini, E
Korge, BP
Ocana-Sierra, J
Calzolari, E
Cambiaghi, S
Scudder, PM
Hovnanian, A
Monaco, AP
Munro, CS
Citation: E. Maestrini et al., A missense mutation in connexin26, D66H, causes mutilating keratoderma with sensorineural deafness (Vohwinkel's syndrome) in three unrelated families, HUM MOL GEN, 8(7), 1999, pp. 1237-1243