Disorders of mitochondrial protein synthesis
Author:
Publisher
Oxford University Press (OUP)
Subject
Genetics(clinical),Genetics,Molecular Biology,General Medicine
Link
http://academic.oup.com/hmg/article-pdf/12/suppl_2/R293/1715315/ddg285.pdf
Reference70 articles.
1. Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies
2. Are duplications of mitochondrial DNA characteristic of Kearns—Sayre syndrome?
3. Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNALys mutation
4. A mutation in the tRNALeu(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies
5. A point mutation in the mitochondrial tRNALeu(UUR) gene in melas (mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes)
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