A Gene for Autosomal Dominant Late-Onset Progressive Non-Syndromic Hearing Loss, DFNA10 , Maps to Chromosome 6

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Human Molecular Genetics, Vol. 5, Iss. 6, 1996-01 ,pp. : 853-856

Oxford University Press

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A targeted Coch missense mutation: a knock-in mouse model for DFNA9 late-onset hearing loss and vestibular dysfunction

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Human Molecular Genetics, Vol. 17, Iss. 21, 2008-11 ,pp. : 3426-3434

Oxford University Press

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A Gene for Non-Syndromic Autosomal Dominant Progressive Postlingual Sensorineural Hearing Loss Maps to Chromosome 14q12–13

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Human Molecular Genetics, Vol. 5, Iss. 7, 1996-01 ,pp. : 1047-1050

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Progressive hearing loss, and recurrent sudden sensorineural hearing loss associated with mutations – phenotypic spectrum and frequencies of mutations in Austria

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Mutations in the WFS1 gene are a frequent cause of autosomal dominant nonsyndromic low-frequency hearing loss in Japanese

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