Mitochondrial disease: recognising more than just the tip of the iceberg
Author:
Affiliation:
1. Department of Neurology, Kolling Institute of Medical Research, Royal North Shore Hospital and University of Sydney, Sydney, NSW.
Publisher
AMPCo
Subject
General Medicine
Link
https://onlinelibrary.wiley.com/doi/pdf/10.5694/j.1326-5377.2010.tb03864.x
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4. Extremely high levels of mutant mtDNAs co-localize with cytocohrome c oxidase-negative ragged-red fibers in patients harboring a point mutation at nt 3243
5. The mitochondrial DNA transfer RNALeu(UUR) A→ G(3243) mutation. A clinical and genetic study;Hammans SR;Brain,1995
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