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April 1, 1992Annals of Neurology

MELAS: Clinical features, biochemistry, and molecular genetics

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Authors

ECEmma CiafaloniUniversity of Rochester Medical CenterEREnzo RicciHeart Failure & TransplantSSSara ShanskeColumbia University Irving Medical Center

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Cite This Study

Ciafaloni et al. (1992) studied this question.

synapsesocial.com/papers/6a63db83de6e3d49e3f2dce9https://doi.org/10.1002/ana.410310408
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Also Consider

Synapse has enriched 4 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Mitochondrial DNA Deletions in Progressive External Ophthalmoplegia and Kearns-Sayre Syndrome1989 · 1,034 citations
  2. 2Deletions of mitochondrial DNA in Kearns‐Sayre syndrome1988 · 740 citations
  3. 3Widespread tissue distribution of a tRNA <sup>Leu(UUR)</sup> mutation in the mitochondrial DNA of a patient with MELAS syndrome1991 · 105 citations
  4. 4In vitro genetic transfer of protein synthesis and respiration defects to mitochondrial DNA-less cells with myopathy-patient mitochondria.1991 · 295 citations