Deficiency of the α Subunit of Succinate–Coenzyme A Ligase Causes Fatal Infantile Lactic Acidosis with Mitochondrial DNA Depletion

This publication has 20 references indexed in Scilit:

• SUCLA2 mutations are associated with mild methylmalonic aciduria, Leigh-like encephalomyopathy, dystonia and deafness
  Brain, 2007
• Reconsideration of the significance of substrate-level phosphorylation in the citric acid cycle
  Biochemistry and Molecular Biology Education, 2006
• Deficiency of the ADP-Forming Succinyl-CoA Synthase Activity Is Associated with Encephalomyopathy and Mitochondrial DNA Depletion
  American Journal of Human Genetics, 2005
• Expression of Two Succinyl-CoA Synthetases with Different Nucleotide Specificities in Mammalian Tissues
  Journal of Biological Chemistry, 2004
• POLG mutations associated with Alpers' syndrome and mitochondrial DNA depletion
  Annals of Neurology, 2004
• Thymidine Phosphorylase Gene Mutations in MNGIE, a Human Mitochondrial Disorder
  Science, 1999
• Optimization of genome search strategies for homozygosity mapping: influence of marker spacing on power and threshold criteria for identification of candidate regions
  Annals of Human Genetics, 1998
• Optimization of genome search strategies for homozygosity mapping: influence of marker spacing on power and threshold criteria for identification of candidate regions
  Annals of Human Genetics, 1998
• An Evaluation of the Measurement of the Activities of Complexes I-IV in the Respiratory Chain of Human Skeletal Muscle Mitochondria
  Biochemical Medicine and Metabolic Biology, 1994
• Apparent ATP-linked succinate thiokinase activity and its relation to nucleoside diphosphate kinase in mitochondrial matrix preparations from rabbit
  Biochimica et Biophysica Acta (BBA) - General Subjects, 1991