Inherited susceptibility to aminoglycoside ototoxicity: Genetic heterogeneity and clinical implications
- 1 May 1999
- journal article
- case report
- Published by Elsevier in American Journal of Otolaryngology
- Vol. 20 (3) , 151-156
- https://doi.org/10.1016/s0196-0709(99)90062-5
Abstract
No abstract availableKeywords
This publication has 12 references indexed in Scilit:
- Familial Progressive Sensorineural Deafness Is Mainly Due to the mtDNA A1555G Mutation and Is Enhanced by Treatment with AminoglycosidesAmerican Journal of Human Genetics, 1998
- 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
- Non-Syndromic Deafness Associated with a Mutation and a Polymorphism in the Mitochondrial 12S Ribosomal RNA Gene in a Large Zairean PedigreeEuropean Journal of Human Genetics, 1996
- Mitochondrial mutation associated with nonsyndromic deafnessAmerican Journal of Otolaryngology, 1995
- Susceptibility mutations in the mitochondrial small ribosomal RNA gene in aminoglycoside induced deafnessPharmacogenetics, 1995
- Mitochondrial DNA Variants Observed in Alzheimer Disease and Parkinson Disease PatientsGenomics, 1993
- 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