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