Mutations in SURF1 are not specifically associated with Leigh syndrome

Samankaltaisia teoksia

• A high rate (20%-30%) of parental consanguinity in cytochrome-oxidase deficiency.
  Tekijä: von Kleist-Retzow, J C, et al.
  Julkaistu: (1998)
• 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
  Tekijä: Chol, M, et al.
  Julkaistu: (2003)
• Large-Scale Deletion and Point Mutations of the Nuclear NDUFV1 and NDUFS1 Genes in Mitochondrial Complex I Deficiency
  Tekijä: Bénit, Paule, et al.
  Julkaistu: (2001)
• Mutant NDUFS3 subunit of mitochondrial complex I causes Leigh syndrome
  Tekijä: Benit, P, et al.
  Julkaistu: (2004)
• MR Findings in Leigh Syndrome with COX Deficiency and SURF-1 Mutations
  Tekijä: Farina, Laura, et al.
  Julkaistu: (2002)