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Original Article

Molecular Genetics Applied to Clinical Practice: The Cx26 Hearing Impairment

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Pages 291-295 | Published online: 12 Oct 2009

References

  • Cohn E S. Clinical studies of families with hearing loss attributable to mutations in the connexin 26 gene. Pediatrics 1999; 103: 546–50
  • Denoyelle F, Weil D, Maw A M, Wilcox S A, Lench N J, Allen-Powell D R. Prelingual deafness; high prevalence of a 30delG mutation in the connexin 26 gene. Hum Mol Genet 1997; 6: 2173–7
  • Denoyelle F, Marlin S, Weil D, Moatti L, Chauvin P, Garabedian E. Clinical features of the prevalent form of childhood deafness, DNFB1, due to a connexin-26 gene defect: implications for genetic counselling. Lancet 1999; 353: 1298–1303
  • Estivill X, Fortina P, Surrey S, Rabionet R, Melchionda S, D'Agruma L. Connexin-26 mutations in sporadic and inherited sensorineural deafness. Lancet 1998; 51: 394–8
  • Fortnum H, Davis A. Epidemiology of permanent childhood hearing impairment in the Trent region 1985–1993. Br J Audiol 1997; 31: 409–46
  • Lench N, Houseman M, Newton V, Van Camp G, Mueller R. Connexin 26 mutations in sporadic non-syndromal sensorineural deafness. Lancet 1998; 51: 415
  • Murgia A, Orzan E, Polli R, Martella M, Vinanzi C, Leonardi E. Cx26 deafness: mutation analysis and clinical variability. J Med Genet 1999
  • Zelante L, Gasparini P, Estivill X, Melchionda S, D'Agruma L, Govea N. Connexin 26 mutations associated with the most common form of nonsyndromic neurosensory autosomal recessive deafness DFNB1 in mediterranean's. Hum Mol Genet 1997; 6: 1605–9

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