Longitudinal changes of mtDNA A3243G mutation load and level of functioning in MELAS
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
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3. In vitro genetic transfer of protein synthesis and respiration defects to mitochondrial DNA-less cells with myopathy-patient mitochondria;Chomyn;Mol Cell Biol,1991
4. Widespread tissue distribution of a tRNALeu(UUR) mutation in the mitochondrial DNA of a patient with MELAS syndrome;Ciafaloni;Neurology,1991
5. Mitochondrial encephalomyopathies;DiMauro;Arch Neurol,1993
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