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Audiological Medicine Volume 8, 2010 - Issue 1
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Research Article

Genetic background of candidates for EAS (Electric-Acoustic Stimulation)

Shin-Ichi Usami Department of Otorhinolaryngology, Shinshu University School of Medicine, Matsumoto, JapanCorrespondence[email protected]
,
Maiko Miyagawa Department of Otorhinolaryngology, Shinshu University School of Medicine, Matsumoto, Japan
,
Nobuyoshi Suzuki Department of Otorhinolaryngology, Shinshu University School of Medicine, Matsumoto, Japan
,
Hideaki Moteki Department of Otorhinolaryngology, Shinshu University School of Medicine, Matsumoto, Japan
,
Shin-Ya Nishio Department of Otorhinolaryngology, Shinshu University School of Medicine, Matsumoto, Japan
,
Yutaka Takumi Department of Otorhinolaryngology, Shinshu University School of Medicine, Matsumoto, Japan
&
Satoshi Iwasaki Department of Hearing Implants Sciences, Shinshu University School of Medicine, Matsumoto, Japan
 show all
Pages 28-32 | Accepted 13 Dec 2009, Published online: 03 Feb 2010

References

  • Usami S, Wagatsuma M, Fukuoka H, Suzuki H, Tsukada K, Nishio S, . The responsible genes in Japanese deafness patients and clinical application using Invader assay. Acta Otolaryngol. 2008;128:446–54.
  • Abe S, Usami S, Shinkawa H, Kelley PM, Kimberling WJ. Prevalent Connexin 26 gene (GJB2) mutations in Japanese. J Med Genet. 2000;37:41–3.
  • Usami S, Abe S, Kasai M, Shinkawa H, Moeller B, Kenyon JB, . Genetic and clinical features of sensorineural hearing loss associated with the 1555A>G mitochondrial mutation. Laryngoscope. 1997;107:483–90.
  • Usami S, Abe S, Weston MD, Shinkawa H, van Camp G, Kimberling WJ. Non-syndromic hearing loss associated with enlarged vestibular aqueduct is caused by PDS mutations. Hum Genet. 1999;104:188–92.
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  • Wagatsuma M, Kitoh R, Suzuki H, Fukuoka H, Takumi Y, Usami S. Distribution and frequencies of CDH23 mutations in Japanese patients with non-syndromic hearing loss. Clin Genet. 2007;72:339–44.
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  • Usami S, Abe S, Akita J, Namba A, Shinkawa H, Ishii M, . Prevalence of mitochondrial gene mutations among hearing impaired patients. J Med Genet. 2000;37:38–40.
  • Everett LA, Glaser B, Beck JC, Idol JR, Buchs A, Heyman M, . Pendred syndrome is caused by mutations in a putative sulphate transporter gene (PDS). Nat Genet. 1997;17:411–22.
  • Usami S, Abe S, Weston MD, Shinkawa H, van Camp G, Kimberling WJ. Non-syndromic hearing loss associated with enlarged vestibular aqueduct is caused by PDS mutations. Hum Genet. 1999;104:188–92.
  • Suzuki H, Oshima A, Tsukamoto K, Abe S, Kumakawa K, Nagai K, . Clinical characteristics and genotype-phenotype correlation of hearing loss patients with SLC26A4 mutations. Acta Otolaryngol. 2007;127:1292–7.
  • Bork JM, Peters LM, Riazuddin S, Bernstein SL, Ahmed ZM, Ness SL, . Usher syndrome 1D and non-syndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23. Am J Hum Genet. 2001;68:26–37.
  • Smith RJ, Bale JF Jr, White KR. Sensorineural hearing loss in children. Lancet. 2005;365:879–90.
  • Hilgert N, Smith RJ, van Camp G. Forty-six genes causing non-syndromic hearing impairment: which ones should be analyzed in DNA diagnostics? Mutat Res. 2009;681:189–96.

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