Connexin-26 mutations in sporadic non-syndromal sensorineural deafness
- PMID: 9482297
- DOI: 10.1016/s0140-6736(98)24006-2
Connexin-26 mutations in sporadic non-syndromal sensorineural deafness
Comment in
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Connexin 26 gene mutation and autosomal recessive deafness.Lancet. 1998 Feb 7;351(9100):383-4. doi: 10.1016/S0140-6736(05)78347-1. Lancet. 1998. PMID: 9482285 No abstract available.
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Connexin-26 mutations and inherited deafness.Lancet. 1998 Apr 11;351(9109):1131. doi: 10.1016/s0140-6736(05)79412-5. Lancet. 1998. PMID: 9660606 No abstract available.
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