Associated Papers
Two novel SUCLA2 variants cause mitochondrial DNA depletion syndrome, type 5 in two siblings.
Zhang X et al.
Frontiers in Neurology, 2024
Succinyl-CoA Synthetase Dysfunction as a Mechanism of Mitochondrial Encephalomyopathy: More than Just an Oxidative Energy Deficit.
Lancaster MS et al.
International Journal of Molecular Sciences, 2023
Succinate-CoA ligase deficiency due to mutations in SUCLA2 and SUCLG1: phenotype and genotype correlations in 71 patients.
Carrozzo R et al.
Journal of Inherited Metabolic Disease, 2016
Select a paper to view details