Confirmation that a T-to-C mutation at 9176 in mitochondrial DNA is an additional candidate mutation for Leigh's syndrome

This publication has 9 references indexed in Scilit:

• Leigh syndrome associated with the T9176C mutation in the ATPase 6 gene of mitochondrial DNA
  Neurology, 1997
• Bilateral striatal necrosis with a novel point mutation in the mitochondrial ATPase 6 gene
  Pediatric Neurology, 1995
• A novel mitochondrial ATPase 6 point mutation in familial bilateral striatal necrosis
  Annals of Neurology, 1995
• Recent African origin of modern humans revealed by complete sequences of hominoid mitochondrial DNAs.
  Proceedings of the National Academy of Sciences, 1995
• The mutation at nt 8993 of mitochondrial DNA is a common cause of Leigh's syndrome
  Annals of Neurology, 1993
• A second missense mutation in the mitochondrial ATPase 6 gene in Leigh's syndrome
  Annals of Neurology, 1993
• Mitochondrial DNA mutation and Leigh's syndrome
  Annals of Neurology, 1992
• Variability in the activity of respiratory chain enzymes in mitochondrial myopathies
  Acta Neuropathologica, 1988
• Diagnosis of partial deficiency of the pyruvate dehydrogenase complex in biopsied muscle
  Neurology, 1985