Prevalence of the mitochondrial DNA A1555G mutation in sensorineural deafness patients in island Southeast Asia
- 3 September 2003
- journal article
- research article
- Published by Springer Nature in Journal of Human Genetics
- Vol. 48 (9) , 480-483
- https://doi.org/10.1007/s10038-003-0056-9
Abstract
No abstract availableKeywords
This publication has 28 references indexed in Scilit:
- Prevalence of the mitochondrial DNA A1555G mutation in sensorineural deafness patients in island Southeast AsiaJournal of Human Genetics, 2003
- The A1555G mtDNA mutation in Danish hearing-impaired patients: frequency and clinical signsClinical Genetics, 2002
- Mutation A1555G in the 12S rRNA gene and its epidemiological importance in German, Hungarian, and Polish patientsHuman Mutation, 2002
- Frequency and clinical features of patients with sensorineural hearing loss associated with the A3243G mutation of the mitochondrial DNA in otorhinolaryngic clinicsJournal of Human Genetics, 2001
- Prevalence of mitochondrial gene mutations among hearing impaired patientsJournal of Medical Genetics, 2000
- Challenge of Epidemiological Research in the Developing World: Overview: Reto a la investigacion epidemiológies en el mundo en desarrollo: Una revisionInternational Journal of Audiology, 2000
- Rapid identification of an A1555G mutation in human mitochondrial DNA implicated in aminoglycoside-induced ototoxicityJournal of Human Genetics, 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
- Mitochondrial ribosomal RNA mutation associated with both antibiotic–induced and non–syndromic deafnessNature Genetics, 1993
- Sequence and organization of the human mitochondrial genomeNature, 1981