Two Iranian Families with a Novel Mutation in GJB2 Causing Autosomal Dominant Nonsyndromic Hearing Loss

Por Bazazzadegan, Niloofar, Sheffield, Abraham M., Sobhani, Masoomeh, Kahrizi, Kimia, Meyer, Nicole C, Van Camp, Guy, Hilgert, Nele, Abedini, Seyedeh Sedigheh, Habibi, Farkhondeh, Daneshi, Ahmad, Nishimura, Carla, Avenarius, Matthew R., Farhadi, Mohammad, Smith, Richard J.H., Najmabadi, Hossein
Publicado em 2011