Maternally inherited myopathy and cardiomyopathy: association with mutation in mitochondrial DNA tRNALeu(UUR)
Author:
Publisher
Elsevier BV
Subject
General Medicine
Reference18 articles.
1. Sequence and organization of the human mitochondrial genome;Anderson;Nature,1981
2. Mitochondrial DNA mutation associated with Leber's optic atrophy;Wallace;Science,1988
3. A new mitochondrial disease associated with mitochondrial DNA heteroplasmy;Holt;Am J Hum Genet,1990
4. Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNAlys mutation;Shoffner;Cell,1990
5. A mutation in the tRNAleu(UUR)gene associated with MELAS subgroup of mitochondrial encephalomyopathies;Goto;Nature,1990
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