Mutational analysis of the mitochondrial 12S rRNA gene in Chinese pediatric subjects with aminoglycoside-induced and non-syndromic hearing loss
- 20 April 2005
- journal article
- research article
- Published by Springer Science and Business Media LLC in Human Genetics
- Vol. 117 (1), 9-15
- https://doi.org/10.1007/s00439-005-1276-1
Abstract
No abstract availableKeywords
This publication has 42 references indexed in Scilit:
- Extremely low penetrance of hearing loss in four Chinese families with the mitochondrial 12S rRNA A1555G mutationBiochemical and Biophysical Research Communications, 2005
- Clinical evaluation and sequence analysis of the complete mitochondrial genome of three Chinese patients with hearing impairment associated with the 12S rRNA T1095C mutationBiochemical and Biophysical Research Communications, 2004
- Molecular analysis of the mitochondrial 12S rRNA and tRNASer(UCN) genes in paediatric subjects with non-syndromic hearing lossJournal of Medical Genetics, 2004
- Cosegregation of C‐insertion at position 961 with the A1555G mutation of the mitochondrial 12S rRNA gene in a large Chinese family with maternally inherited hearing lossAmerican Journal of Medical Genetics Part A, 2003
- Mutation A1555G in the 12S rRNA gene and its epidemiological importance in German, Hungarian, and Polish patientsHuman Mutation, 2002
- Maternally inherited deafness associated with a T1095C mutation in the mDNAEuropean Journal of Human Genetics, 2001
- Prevalence of mitochondrial gene mutations among hearing impaired patientsJournal of Medical Genetics, 2000
- Genetic Factors in Aminoglycoside ToxicityAnnals of the New York Academy of Sciences, 1999
- Familial Progressive Sensorineural Deafness Is Mainly Due to the mtDNA A1555G Mutation and Is Enhanced by Treatment with AminoglycosidesAmerican Journal of Human Genetics, 1998
- Genetic aspects of antibiotic induced deafness: mitochondrial inheritance.Journal of Medical Genetics, 1991