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Bazazzadegan, N. and Sheffield, A.M. and Sobhani, M. and Kahrizi, K. and Meyer, N.C. and Van Camp, G. and Hilgert, N. and Abedini, S.S. and Habibi, F. and Daneshi, A. and Nishimura, C. and Avenarius, M.R. and Farhadi, M. and Smith, R.J. and Najmabadi, H. (2011) Two Iranian families with a novel mutation in GJB2 causing autosomal dominant nonsyndromic hearing loss. American Journal of Medical Genetics, Part A, 155 (5). pp. 1202-1211.
