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June 10, 2003Neurology

A missense mutation in the mitochondrial ND5 gene associated with a Leigh-MELAS overlap syndrome

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MCMarco CrimiUniversity of BergamoSGSara GalbiatiIRCCS Eugenio MedeaIMIsabella MoroniUniCredit (Italy)

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Crimi et al. (2003) studied this question.

synapsesocial.com/papers/6aaba991ae7d76820a16de92https://doi.org/10.1212/01.wnl.0000066048.72780.69
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Also Consider

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

  1. 1The mitochondrial DNA G13513A transition in ND5 is associated with a LHON/MELAS overlap syndrome and may be a frequent cause of MELAS1999 · 118 citations
  2. 2MELAS syndrome1988 · 182 citations
  3. 3Mitochondrial disease associated with the T8993G mutation of the mitochondrial ATPase 6 gene: a clinical, biochemical, and molecular study in six families1997 · 154 citations
  4. 4Respiratory chain complex I deficiency2001 · 189 citations