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Volumn 132, Issue 6, 2005, Pages 890-895

Etiologic diagnosis of sensorineural hearing loss in adults

Author keywords

[No Author keywords available]

Indexed keywords

GAP JUNCTION PROTEIN; GAP JUNCTION PROTEIN BETA2; MITOCHONDRIAL DNA; UNCLASSIFIED DRUG;

EID: 20444406829     PISSN: 01945998     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.otohns.2005.03.001     Document Type: Article
Times cited : (18)

References (17)
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  • 5
    • 0028288558 scopus 로고
    • A novel mitochondrial point mutation in a maternal pedigree with sensorineural deafness
    • F.M. Reid, G.A. Vernham, H.T. Jacobs A novel mitochondrial point mutation in a maternal pedigree with sensorineural deafness Hum Mutat 3 1994 243 247
    • (1994) Hum Mutat , vol.3 , pp. 243-247
    • Reid, F.M.1    Vernham, G.A.2    Jacobs, H.T.3
  • 7
    • 17344365276 scopus 로고    scopus 로고
    • Familial progressive sensorineural deafness is mainly due to the mtDNA A1555G mutation and is enhanced by treatment with aminoglycosides
    • X. Estivill, N. Govea, A. Barcelo Familial progressive sensorineural deafness is mainly due to the mtDNA A1555G mutation and is enhanced by treatment with aminoglycosides Am J Genet 62 1998 27 35
    • (1998) Am J Genet , vol.62 , pp. 27-35
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  • 8
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    • (2000) J Med Genet , vol.37 , pp. 38-40
    • Usami, S.1    Abe, S.2    Akita, J.3
  • 9
    • 84869588963 scopus 로고    scopus 로고
    • Recommendations for the description of genetic and audiological data for families with nonsyndromic hereditary hearing impairment
    • Van Camp G, Smith RJH, Editors.
    • Mazzoli M, Van Camp G, Newton V, et al. Recommendations for the description of genetic and audiological data for families with nonsyndromic hereditary hearing impairment. In: Van Camp G, Smith RJH, editors. Hereditary hearing loss homepage. URL: http://dnalab-www.uia.ac.be/dnalab/hhh/. Last accessed August 10, 2004.
    • Hereditary Hearing Loss Homepage
    • Mazzoli, M.1    Van Camp, G.2    Newton, V.3
  • 10
    • 0031055387 scopus 로고    scopus 로고
    • Mutation in the mitochondrial 12S rRNA gene in two families from Mongolia with matrilineal aminoglycoside ototoxicity
    • A. Pandya, X. Xia, J. Radnaabazar Mutation in the mitochondrial 12S rRNA gene in two families from Mongolia with matrilineal aminoglycoside ototoxicity J Med Genet 34 1997 169 172
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    • Scott, D.A.1    Kraft, M.L.2    Carmi, R.3
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.