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.
4Anderson.S,Bankier.AT,Barrell.BG and et al.Sequence and organization of the humanmitochondrial genome[J].Nature,1981,290:457.
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.
7Shoffner JM,Lott MT,Lezza AMS, et al.Myoclonic epilepsy and ragged-red feberdisease (NERRF) is assicuated with a mitochondial DNA tRNALysmutation[J].Cell,1990,61:931.
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.