SUCLA2 mutations cause global protein succinylation contributing to the pathomechanism of a hereditary mitochondrial disease | Nature Communications
IJMS | Free Full-Text | Succinyl-CoA Synthetase Dysfunction as a Mechanism of Mitochondrial Encephalomyopathy: More than Just an Oxidative Energy Deficit
SUCLA2 Antibody (NBP1-33015): Novus Biologicals
SUCLA2 mutations cause global protein succinylation contributing to the pathomechanism of a hereditary mitochondrial disease | Nature Communications
Disorders caused by deficiency of succinate‐CoA ligase - Ostergaard - 2008 - Journal of Inherited Metabolic Disease - Wiley Online Library
SUCLA2 mutations cause global protein succinylation contributing to the pathomechanism of a hereditary mitochondrial disease | Nature Communications