Novel Mitochondrial DNA ND5 Mutation in a Patient With Clinical Features of MELAS and MERRF

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Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

1. 1Recurrent brain hematomas in MELAS associated with an ND5 gene mitochondrial mutation2000 · 45 citations
2. 2The 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
3. 3A missense mutation in the mitochondrial ND5 gene associated with a Leigh-MELAS overlap syndrome2003 · 75 citations
4. 4Is the mitochondrial complex I ND5 gene a hot‐spot for MELAS causing mutations?2002 · 124 citations
5. 5Identification of a Novel Mutation in the mtDNA ND5 Gene Associated with MELAS1997 · 171 citations