Connexin 26 gene mutation and autosomal recessive deafness

W Reardon¹

Affiliations

Comment

W Reardon. Lancet. 1998.

. 1998 Feb 7;351(9100):383-4.

doi: 10.1016/S0140-6736(05)78347-1.

W Reardon¹

¹ Department of Clinical Genetics and Fetal Medicine, Institute of Child Health, London, UK.

No abstract available

Comment on

Connexin-26 mutations in sporadic and inherited sensorineural deafness.
Estivill X, Fortina P, Surrey S, Rabionet R, Melchionda S, D'Agruma L, Mansfield E, Rappaport E, Govea N, Milà M, Zelante L, Gasparini P. Estivill X, et al. Lancet. 1998 Feb 7;351(9100):394-8. doi: 10.1016/S0140-6736(97)11124-2. Lancet. 1998. PMID: 9482292
Connexin-26 mutations in sporadic non-syndromal sensorineural deafness.
Lench N, Houseman M, Newton V, Van Camp G, Mueller R. Lench N, et al. Lancet. 1998 Feb 7;351(9100):415. doi: 10.1016/s0140-6736(98)24006-2. Lancet. 1998. PMID: 9482297 No abstract available.