The G13513A mutation in the ND5 gene of mitochondrial DNA as a common cause of MELAS or Leigh syndrome: evidence from 12 cases.

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Synapse has enriched 5 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. 2Identification of a Novel Mutation in the mtDNA ND5 Gene Associated with MELAS1997 · 171 citations
3. 3Novel Mitochondrial DNA ND5 Mutation in a Patient With Clinical Features of MELAS and MERRF2005 · 78 citations
4. 4A novel mtDNA mutation in the ND5 subunit of complex I in two MELAS patients2001 · 110 citations
5. 5The mitochondrial DNA G13513A MELAS mutation in the NADH dehydrogenase 5 gene is a frequent cause of Leigh-like syndrome with isolated complex I deficiency2003 · 154 citations