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DFNA25, a novel locus for dominant nonsyndromic hereditary hearing impairment, maps to 12q21-24.
Am J Hum Genet. 2001 Jan;68(1):254-60. doi: 10.1086/316925. Epub 2000 Dec 11.
Am J Hum Genet. 2001.
PMID: 11115382
Free PMC article.
Mutations in the Wolfram syndrome 1 gene (WFS1) are a common cause of low frequency sensorineural hearing loss.
Bespalova IN, Van Camp G, Bom SJ, Brown DJ, Cryns K, DeWan AT, Erson AE, Flothmann K, Kunst HP, Kurnool P, Sivakumaran TA, Cremers CW, Leal SM, Burmeister M, Lesperance MM.
Bespalova IN, et al. Among authors: kurnool p.
Hum Mol Genet. 2001 Oct 15;10(22):2501-8. doi: 10.1093/hmg/10.22.2501.
Hum Mol Genet. 2001.
PMID: 11709537
Free PMC article.
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