The mitochondrial DNA G13513A MELAS mutation in the NADH dehydrogenase 5 gene is a frequent cause of Leigh-like syndrome with isolated complex I deficiency

Gelijkaardige items

• Mutant NDUFS3 subunit of mitochondrial complex I causes Leigh syndrome
  door: Benit, P, et al.
  Gepubliceerd in: (2004)
• Recurrent de novo mitochondrial DNA mutations in respiratory chain deficiency
  door: Lebon, S, et al.
  Gepubliceerd in: (2003)
• Mutations in SURF1 are not specifically associated with Leigh syndrome
  door: VON KLEIST-RETZOW, J.-C., et al.
  Gepubliceerd in: (2001)
• Large-Scale Deletion and Point Mutations of the Nuclear NDUFV1 and NDUFS1 Genes in Mitochondrial Complex I Deficiency
  door: Bénit, Paule, et al.
  Gepubliceerd in: (2001)
• A high rate (20%-30%) of parental consanguinity in cytochrome-oxidase deficiency.
  door: von Kleist-Retzow, J C, et al.
  Gepubliceerd in: (1998)