Mutant NDUFS3 subunit of mitochondrial complex I causes Leigh syndrome

Antzeko izenburuak

• 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
  nork: Chol, M, et al.
  Argitaratua: (2003)
• Recurrent de novo mitochondrial DNA mutations in respiratory chain deficiency
  nork: Lebon, S, et al.
  Argitaratua: (2003)
• Large-Scale Deletion and Point Mutations of the Nuclear NDUFV1 and NDUFS1 Genes in Mitochondrial Complex I Deficiency
  nork: Bénit, Paule, et al.
  Argitaratua: (2001)
• Mutations in SURF1 are not specifically associated with Leigh syndrome
  nork: VON KLEIST-RETZOW, J.-C., et al.
  Argitaratua: (2001)
• Late-onset Leigh syndrome in a patient with mitochondrial complex I NDUFS8 mutations
  nork: Procaccio, Vincent, et al.
  Argitaratua: (2004)