Pathogenesis of the deafness-associated A1555G mitochondrial DNA mutation
- 26 April 2002
- journal article
- case report
- Published by Elsevier in Biochemical and Biophysical Research Communications
- Vol. 293 (1), 521-529
- https://doi.org/10.1016/s0006-291x(02)00256-5
Abstract
No abstract availableKeywords
This publication has 47 references indexed in Scilit:
- Mitochondrial defects and hearing lossCellular and Molecular Life Sciences, 2000
- Maternally inherited hearing impairmentClinical Genetics, 2000
- Genetic Causes of Hearing LossNew England Journal of Medicine, 2000
- Mitochondrial gene mutation is a significant predisposing factor in aminoglycoside ototoxicityAmerican Journal of Otolaryngology, 1997
- Mutation in the mitochondrial 12S rRNA gene in two families from Mongolia with matrilineal aminoglycoside ototoxicity.Journal of Medical Genetics, 1997
- Two large Spanish pedigrees with nonsyndromic sensorineural deafness and the mtDNA mutation at nt 1555 in the 12S rRNA geneNeurology, 1997
- Maternally inherited hearing loss, ataxia and myoclonus associated with a novel point mutation in mitochondrial tRNA Ser(UCN) geneHuman Molecular Genetics, 1995
- A novel mitochondrial point mutation in a maternal pedigree with sensorineural deafnessHuman Mutation, 1994
- Mitochondrial ribosomal RNA mutation associated with both antibiotic–induced and non–syndromic deafnessNature Genetics, 1993
- A Molecular basis for human hypersensitivity of aminoglyscoside antibioticsNucleic Acids Research, 1993