Identification of mutations in the Connexin 26 gene that cause autosomal recessive nonsyndromic hearing loss

D. A. Scott, M. L. Kraft, R. Carmi, A. Ramesh, K. Elbedour, Y. Yairi, C. R. Srikumari Srisailapathy, S. S. Rosengren, A. F. Markham, R. F. Mueller, N. J. Lench, G. Van Camp, R. J.H. Smith, V. C. Sheffield

Research output: Contribution to journal › Article › peer-review

213 Scopus citations

Fingerprint

Dive into the research topics of 'Identification of mutations in the Connexin 26 gene that cause autosomal recessive nonsyndromic hearing loss'. Together they form a unique fingerprint.

Keyphrases

Biochemistry, Genetics and Molecular Biology