Heterogenous point mutations in the mitochondrial tRNA Ser(UCN) precursor coexisting with the A1555G mutation in deaf students from Mongolia

[1] SEQUENCE AND ORGANIZATION OF THE HUMAN MITOCHONDRIAL GENOME [J]. NATURE, 1981, 290 (5806) : 457 - 465

[2] PHYLOGENETIC ANALYSIS OF LEBERS HEREDITARY OPTIC NEUROPATHY MITOCHONDRIAL DNAS INDICATES MULTIPLE INDEPENDENT OCCURRENCES OF THE COMMON MUTATIONS [J]. HUMAN MUTATION, 1995, 6 (04) : 311 - 325

[3] Bykhovskaya Y, 1998, AM J MED GENET, V77, P421, DOI 10.1002/(SICI)1096-8628(19980605)77:5<421::AID-AJMG13>3.0.CO

[4] 2-K

[5] Familial progressive sensorineural deafness is mainly due to the mtDNA A1555G mutation and is enhanced by treatment with aminoglycosides [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 1998, 62 (01) : 27 - 35

[6] The deafness-associated mitochondrial DNA mutation at position 7445, which affects tRNASer(UCN) precursor processing, has long-range effects on NADH dehydrogenase subunit ND6 gene expression [J]. MOLECULAR AND CELLULAR BIOLOGY, 1998, 18 (10) : 5868 - 5879

[7] Biochemical evidence for nuclear gene involvement phenotype of non-syndromic deafness associated with mitochondrial 12S rRNA mutation [J]. HUMAN MOLECULAR GENETICS, 1996, 5 (07) : 963 - 971

[8] Specific binding of aminoglycosides to a human rRNA construct based on a DNA polymorphism which causes aminoglycoside-induced deafness [J]. BIOCHEMISTRY, 1997, 36 (40) : 12323 - 12328

[9] HANKE M, 1994, BIOTECHNIQUES, V17, P858

[10] HIGASHI K, 1989, CLIN GENET, V35, P433

[1] SEQUENCE AND ORGANIZATION OF THE HUMAN MITOCHONDRIAL GENOME [J]. NATURE, 1981, 290 (5806) : 457 - 465

[2] PHYLOGENETIC ANALYSIS OF LEBERS HEREDITARY OPTIC NEUROPATHY MITOCHONDRIAL DNAS INDICATES MULTIPLE INDEPENDENT OCCURRENCES OF THE COMMON MUTATIONS [J]. HUMAN MUTATION, 1995, 6 (04) : 311 - 325

[3] Bykhovskaya Y, 1998, AM J MED GENET, V77, P421, DOI 10.1002/(SICI)1096-8628(19980605)77:5<421::AID-AJMG13>3.0.CO

[4] 2-K

[5] Familial progressive sensorineural deafness is mainly due to the mtDNA A1555G mutation and is enhanced by treatment with aminoglycosides [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 1998, 62 (01) : 27 - 35

[6] The deafness-associated mitochondrial DNA mutation at position 7445, which affects tRNASer(UCN) precursor processing, has long-range effects on NADH dehydrogenase subunit ND6 gene expression [J]. MOLECULAR AND CELLULAR BIOLOGY, 1998, 18 (10) : 5868 - 5879

[7] Biochemical evidence for nuclear gene involvement phenotype of non-syndromic deafness associated with mitochondrial 12S rRNA mutation [J]. HUMAN MOLECULAR GENETICS, 1996, 5 (07) : 963 - 971

[8] Specific binding of aminoglycosides to a human rRNA construct based on a DNA polymorphism which causes aminoglycoside-induced deafness [J]. BIOCHEMISTRY, 1997, 36 (40) : 12323 - 12328

[9] HANKE M, 1994, BIOTECHNIQUES, V17, P858

[10] HIGASHI K, 1989, CLIN GENET, V35, P433