Mitochondrial mutations and hearing loss: paradigm for mitochondrial genetics
- PMID: 9443888
- PMCID: PMC1376819
- DOI: 10.1086/301695
Mitochondrial mutations and hearing loss: paradigm for mitochondrial genetics
Comment on
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Familial progressive sensorineural deafness is mainly due to the mtDNA A1555G mutation and is enhanced by treatment of aminoglycosides.Am J Hum Genet. 1998 Jan;62(1):27-35. doi: 10.1086/301676. Am J Hum Genet. 1998. PMID: 9490575 Free PMC article.
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