Specializati Halbă Sancţiune sucla2 punct culminant Despre setare Agitaţie
SUCLA2 antibody (12627-1-AP) | Proteintech
SUCLA2 Antibody (ABIN2856701)
Depletion of mtDNA with MMA: SUCLA2 and SUCLG1 | SpringerLink
Dystonia and deafness due to SUCLA2 defect; Clinical course and biochemical markers in 16 children - ScienceDirect
IJMS | Free Full-Text | Succinyl-CoA Synthetase Dysfunction as a Mechanism of Mitochondrial Encephalomyopathy: More than Just an Oxidative Energy Deficit
SUCLA2 Fusion Protein Ag3319 | Proteintech
Disorders caused by deficiency of succinate‐CoA ligase - Ostergaard - 2008 - Journal of Inherited Metabolic Disease - Wiley Online Library
The GABA Transaminase, ABAT, Is Essential for Mitochondrial Nucleoside Metabolism
Succinyl-CoA Ligase Deficiency: A Mitochondrial Hepatoencephalomyopathy | Pediatric Research
PDF) SUCLA2 mutations are associated with mild methylmalonic aciduria, Leigh-like encephalomyopathy, dystonia and deafness