Audiological and genetic features of themtDNA mutations
Author:
Publisher
Informa UK Limited
Subject
Otorhinolaryngology,General Medicine
Link
http://www.tandfonline.com/doi/pdf/10.1080/00016480701719011
Reference46 articles.
1. Connexin 26 mutations in hereditary non-syndromic sensorineural deafness
2. Mitochondrial ribosomal RNA mutation associated with both antibiotic–induced and non–syndromic deafness
3. Familial Progressive Sensorineural Deafness Is Mainly Due to the mtDNA A1555G Mutation and Is Enhanced by Treatment with Aminoglycosides
4. Mitochondrial Mutations and Hearing Loss: Paradigm for Mitochondrial Genetics
5. Genetic aspects of antibiotic induced deafness: mitochondrial inheritance.
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