A novel mitochondrial 12SrRNA point mutation in parkinsonism, deafness, and neuropathy
Author:
Publisher
Wiley
Subject
Neurology (clinical),Neurology
Reference37 articles.
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3. A novel mitochondrial point mutation in a maternal pedigree with sensorineural deafness
4. Maternally inherited hearing loss, ataxia and myoclonus associated with a novel point mutation in mitochondrial tRNA Ser(UCN) gene
5. Maternally inherited hearing loss in a large kindred with a novel T7511C mutation in the mitochondrial DNA tRNASer(UCN) gene
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