메뉴 건너뛰기




Volumn 43, Issue 6, 2002, Pages 330-333

Screening of mitochondrial DNA mutations in subjects with non-syndromic familial hearing impairment in Taiwan

Author keywords

Mitochondrial DNA mutation; Non syndromic hearing impairment

Indexed keywords

AMINOGLYCOSIDE ANTIBIOTIC AGENT; MITOCHONDRIAL DNA;

EID: 0036876068     PISSN: 16088115     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (9)

References (13)
  • 1
    • 0032549816 scopus 로고    scopus 로고
    • Progress in progressive hearing loss
    • Steel KP. Progress in progressive hearing loss. Science 1998; 279:1870-71.
    • (1998) Science , vol.279 , pp. 1870-1871
    • Steel, K.P.1
  • 2
    • 0012901781 scopus 로고    scopus 로고
    • Van Camp G, Smith RJH. Hereditary hearing loss Home page. http://dnalab-www.uia.ac.be/dnalab/hhh (2002).
    • (2002)
    • Van Camp, G.1    Smith, R.J.H.2
  • 3
    • 0034114952 scopus 로고    scopus 로고
    • Maternally inherited hearing impairment
    • Van Camp G, Smith RJH. Maternally inherited hearing impairment. Clin Genet 2000; 57:409-14.
    • (2000) Clin Genet , vol.57 , pp. 409-414
    • Van Camp, G.1    Smith, R.J.H.2
  • 4
    • 0033058511 scopus 로고    scopus 로고
    • Mitochondrial deafness mutation review
    • Fishchel-Ghodsian N. Mitochondrial deafness mutation review. Hum Mutat 1999; 13:2611-70.
    • (1999) Hum Mutat , vol.13 , pp. 2611-2670
    • Fishchel-Ghodsian, N.1
  • 5
    • 0029003553 scopus 로고
    • Susceptibility mutations in the mitochondrial small ribosomal RNA gene in aminoglycoside-induced deafness
    • Bacino CM, Prezant TR, Bu X, et al. Susceptibility mutations in the mitochondrial small ribosomal RNA gene in aminoglycoside-induced deafness. Pharmacogenetics 1995; 5:165-72.
    • (1995) Pharmacogenetics , vol.5 , pp. 165-172
    • Bacino, C.M.1    Prezant, T.R.2    Bu, X.3
  • 6
    • 0027226069 scopus 로고
    • Mitochondrial ribosomal RNA mutation associated with both antibiotic-induced and non-syndromic deafness
    • Prezant TR, Agapian JV, Bohlman MC, et al. Mitochondrial ribosomal RNA mutation associated with both antibiotic-induced and non-syndromic deafness. Nat Genet 1993; 4:289-94.
    • (1993) Nat Genet , vol.4 , pp. 289-294
    • Prezant, T.R.1    Agapian, J.V.2    Bohlman, M.C.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 aminoglycoside
    • Estivill X, Govea N, Barcelo A, et al. Familial progressive sensorineural deafness is mainly due to the mtDNA A1555G mutation and is enhanced by treatment with aminoglycoside. Am J Hum Genet 1998; 62:27-35.
    • (1998) Am J Hum Genet , vol.62 , pp. 27-35
    • Estivill, X.1    Govea, N.2    Barcelo, A.3
  • 9
    • 0032977958 scopus 로고    scopus 로고
    • Sensorineural hearing loss and the 1555G mitochondrial DNA mutation
    • Hutchin T. Sensorineural hearing loss and the 1555G mitochondrial DNA mutation. Acta Otolaryngol (Stockh) 1999; 119:48-52.
    • (1999) Acta Otolaryngol (Stockh) , vol.119 , pp. 48-52
    • Hutchin, T.1
  • 11
    • 0027515721 scopus 로고
    • Mitochondrial ribosomal RNA gene mutation in a patient with sporadic aminoglycoside ototoxicity
    • Fischel-Ghodsian N, Prezant TR, Bu X, Oztas S. Mitochondrial ribosomal RNA gene mutation in a patient with sporadic aminoglycoside ototoxicity. Am J Otolaryngol 1993; 14:399-403.
    • (1993) Am J Otolaryngol , vol.14 , pp. 399-403
    • Fischel-Ghodsian, N.1    Prezant, T.R.2    Bu, X.3    Oztas, S.4
  • 12
    • 0033362169 scopus 로고    scopus 로고
    • Ser(UCN) precursor coexisting with the A1555G mutation in deaf students from Mongolia
    • Ser(UCN) precursor coexisting with the A1555G mutation in deaf students from Mongolia. Am J Hum Genet 1999; 65:1803-6.
    • (1999) Am J Hum Genet , vol.65 , pp. 1803-1806
    • Pendya, A.1    Xia-Juan, X.2    Erdenetungalag, R.3
  • 13
    • 0012901960 scopus 로고    scopus 로고
    • Connexin 26 gene (GJB2) mutation modulates the severity of hearing loss associated with the 1555A→G mitochondrial mutation
    • Abe S, Kelley PM, Kimberling WJ, et al. Connexin 26 gene (GJB2) mutation modulates the severity of hearing loss associated with the 1555A→G mitochondrial mutation. Am J
    • Am J
    • Abe, S.1    Kelley, P.M.2    Kimberling, W.J.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.