Mitochondrial A3243G mutation causes mitochondrial encephalomyopathy in a Chinese patient
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
General Medicine
Reference13 articles.
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4. A mutation in PNPT1, encoding mitochondrial-RNA-import protein PNPase, causes hereditary hearing loss;von Ameln;Am J Hum Genet,2012
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