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Comment

. 1998 Apr 11;351(9109):1131.

doi: 10.1016/s0140-6736(05)79412-5.

Connexin-26 mutations and inherited deafness

M Parker, H Fortnum, I D Young

PMID: 9660606
DOI: 10.1016/s0140-6736(05)79412-5

Comment

Connexin-26 mutations and inherited deafness

M Parker et al. Lancet. 1998.

. 1998 Apr 11;351(9109):1131.

doi: 10.1016/s0140-6736(05)79412-5.

Authors

M Parker, H Fortnum, I D Young

PMID: 9660606
DOI: 10.1016/s0140-6736(05)79412-5

No abstract available

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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.

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