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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Mutations in the Wolfram syndrome 1 gene ( WFS1 ) are a common cause of low frequency sensorineural hearing loss

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Human Molecular Genetics, Vol. 10, Iss. 22, 2001-10 ,pp. : 2501-2508

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

Oxford University Press

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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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Journal of Human Genetics, Vol. 52, Iss. 6, 2007-06 ,pp. : 510-515

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A novel mutation within the MIR96 gene causes non-syndromic inherited hearing loss in an Italian family by altering pre-miRNA processing

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