IJMS | Free Full-Text | Succinyl-CoA Synthetase Dysfunction as a Mechanism of Mitochondrial Encephalomyopathy: More than Just an Oxidative Energy Deficit
SUCLA2 Polyclonal Antibody (PA5-118292)
Succinyl-CoA ligase ADP-forming subunit beta promotes stress granule assembly to regulate redox and drive cancer metastasis | PNAS
Analysis of the effects of SUCLA2 missense mutations on the structure... | Download Scientific Diagram
Succinyl-CoA Ligase Deficiency: A Mitochondrial Hepatoencephalomyopathy | Pediatric Research
Targeting metabolic vulnerability in advanced prostate cancer | Cancer Community
Clinical and molecular features of mitochondrial DNA depletion syndromes - Spinazzola - 2009 - Journal of Inherited Metabolic Disease - Wiley Online Library
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
Cranial MRI of MDS. Cranial MRI of the patient with SUCLA2 mutation... | Download Scientific Diagram