Mutant NDUFS3 subunit of mitochondrial complex I causes Leigh syndrome

Ítems similars

• 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
  per: Chol, M, et al.
  Publicat: (2003)
• Recurrent de novo mitochondrial DNA mutations in respiratory chain deficiency
  per: Lebon, S, et al.
  Publicat: (2003)
• Large-Scale Deletion and Point Mutations of the Nuclear NDUFV1 and NDUFS1 Genes in Mitochondrial Complex I Deficiency
  per: Bénit, Paule, et al.
  Publicat: (2001)
• Mutations in SURF1 are not specifically associated with Leigh syndrome
  per: VON KLEIST-RETZOW, J.-C., et al.
  Publicat: (2001)
• Mitochondrial DNA inheritance in patients with deleted mtDNA
  per: Quintana-Murci, L., et al.
  Publicat: (2001)