IJMS | Free Full-Text | Succinyl-CoA Synthetase Dysfunction as a Mechanism of Mitochondrial Encephalomyopathy: More than Just an Oxidative Energy Deficit
SUCLA2 gene | Semantic Scholar
Governing glutaminolysis by regulation of glutaminase succinylation | Protein & Cell
SUCLA2 CRISPR Knockout and Activation Products (m) | SCBT - Santa Cruz Biotechnology
Depletion of mtDNA with MMA: SUCLA2 and SUCLG1 | SpringerLink
SUCLA2-coupled regulation of GLS succinylation and activity counteracts oxidative stress in tumor cells - ScienceDirect
Dystonia and deafness due to SUCLA2 defect; Clinical course and biochemical markers in 16 children - ScienceDirect
Analysis of the effects of SUCLA2 missense mutations on the structure... | Download Scientific Diagram
SUCLA2 Antibody (NBP1-33015): Novus Biologicals
PDF) SUCLA2 mutations are associated with mild methylmalonic aciduria, Leigh-like encephalomyopathy, dystonia and deafness