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线粒体DNA突变与感音神经性聋 被引量:1

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出处 《听力学及言语疾病杂志》 CAS CSCD 2000年第4期244-246,共3页 Journal of Audiology and Speech Pathology
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参考文献17

  • 1Jacobs H T.Mitochondrialdeafness[J].Ann Med,1997,29 483.
  • 2Fischel-Ghodsian.Mitochondrial mutations and hearing loss:paradigm formitochondrial genetics.Am.J.Hum[J].Genet,1998,62:15.
  • 3Fischel-Ghodsian.Mitochondrial genetics and hearing loss:the missing link betweengenotype and phenotype[J].PSEBM,1998,218.
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  • 5Moraes CT,Dimauro S,Zeviani M,and et al.Mitochondrial DNA deletions in progressiveexternnal ophthalmoplegia and Kearns-Sayre syndrome[J].N eng1 J Med,1989,320:1293.
  • 6Goto Y,Nonaka I,Norai S.A mutation in the tRNALeu(UUR) gene associated with theMELAS subgroup of mitochondrial encephalomyopathies[J].Nature, 1990,348:651.
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  • 8Syzyki S,hinokio Y,Ohtomo M et al.The effects of coenzyme Q10 treatment onmaterrnally inherited diabetes mellitus and deafness,and mitochondrial DNA 3243(A toG)mutation[J].Diabetologia,1998,41(5):584.
  • 9Prezant TR,Agapian JV,Bohman MC, et al.Mitochondrial ribosomal RNA mutationassociated with both antibiotic-induced and nondynsromic deafness[J].Nat Genet,1993,4:289.
  • 10袁慧军,姜泗长,杨伟炎,郭维维,曹菊阳,杨卫平,戴朴.氨基糖甙类抗生素致聋家系线粒体DNA1555G点突变分析[J].中华耳鼻咽喉科杂志,1998,33(2):67-70. 被引量:32

二级参考文献4

  • 1卢圣栋,现代分子生物学实验技术,1993年,415页
  • 2Hu D N,J Med Genet,1991年,28卷,79页
  • 3袁慧军,中华耳鼻咽喉科杂志,1998年,33卷,67页
  • 4童坦君,医学老年学.衰老与长寿,1995年,142页

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