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Volumn 74, Issue 5, 2008, Pages 786-789

Study of a Brazilian family presenting non-syndromic hearing loss with mitochondrial inheritance;Estudo de família brasileira portadora de deficiência auditiva sensorioneural não-sindrômica com herança mitocondrial

Author keywords

Genetics; Hearing loss; Mitochondrial inheritance; Nonsyndromic hereditary deafness

Indexed keywords

RNA 12S;

EID: 60549107901     PISSN: 18088694     EISSN: 18088686     Source Type: Journal    
DOI: 10.1016/S1808-8694(15)31392-6     Document Type: Article
Times cited : (7)

References (13)
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    • Malik, S.G.1    Pieter, N.2    Sudoyo, H.3    Kadir, A.4    Marzuki, S.5
  • 4
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    • As deficiências auditivas relacionadas às alterações do DNA mitocondrial.
    • Carvalho MFP, Ribeiro FAQ. As deficiências auditivas relacionadas às alterações do DNA mitocondrial. Rev Bras Otorrinolaringol 2002;68(2):268-75.
    • (2002) Rev Bras Otorrinolaringol , vol.68 , Issue.2 , pp. 268-275
    • Carvalho, M.F.P.1    Ribeiro, F.A.Q.2
  • 7
    • 2142699720 scopus 로고    scopus 로고
    • Xing G, Bu X, Yan M. Audiological findings and mitochondrial DNA mutation in a large family with matrilineal sensorineural hearing loss. Zhonghua Er Bi Yan Hou Ke Za Zhi. Clin J Otorhinolaryngol 2000;35(2):98-101.
    • Xing G, Bu X, Yan M. Audiological findings and mitochondrial DNA mutation in a large family with matrilineal sensorineural hearing loss. Zhonghua Er Bi Yan Hou Ke Za Zhi. Clin J Otorhinolaryngol 2000;35(2):98-101.
  • 8
    • 0032168489 scopus 로고    scopus 로고
    • Sensorineural hearing loss caused by mitochondrial DNA mutations: Special reference to the A1555G mutation
    • Usami S, Abe S, Shinkawa H, Kimberling W. Sensorineural hearing loss caused by mitochondrial DNA mutations: special reference to the A1555G mutation. J Commun Disord 1998;(31):423-35.
    • (1998) J Commun Disord , vol.31 , pp. 423-435
    • Usami, S.1    Abe, S.2    Shinkawa, H.3    Kimberling, W.4
  • 10
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    • The A1555G mtDNA mutation in Danish hearing-impaired patients: Frequency and clinical signs
    • Østergaard E, Montserrat-Sentis B, Grønskov K, Brøndum-Nielsen K. The A1555G mtDNA mutation in Danish hearing-impaired patients: frequency and clinical signs. Clin Genet 2002;(62):303-5.
    • (2002) Clin Genet , vol.62 , pp. 303-305
    • Østergaard, E.1    Montserrat-Sentis, B.2    Grønskov, K.3    Brøndum-Nielsen, K.4
  • 13
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    • Familial progressive sensorineural deafness is mainly due to the mtDNA A1555G mutation and is enhanced by treatment of aminoglycosides
    • Estivill X, Govea N, Barcelo E, Badenas C, Romero E, Moral L et al. Familial progressive sensorineural deafness is mainly due to the mtDNA A1555G mutation and is enhanced by treatment of aminoglycosides. 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, E.3    Badenas, C.4    Romero, E.5    Moral, L.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.