QuickView for SUCLG1;jsessionid=DE21CE054782BA308201C127F125EF1D;jsessionid=4A874CFD6189E76D087140613F0BC463;jsessionid=665276D51204178A15A093CF19B21511;jsessionid=FB0FBB4D83C400EFE20BCDF2677BBABD;jsessionid=6B09291086A036E5721463DE0E5F90AF (gene)

1. SUCLG1 mutations and mitochondrial encephalomyopathy: a case study and review of the literature.
2. Expanding the phenotypic spectrum of Succinyl-CoA ligase deficiency through functional validation of…
3. Succinate-CoA ligase deficiency due to mutations in SUCLA2 and SUCLG1: phenotype and genotype correl…
4. SUCLG1 restricts POLRMT succinylation to enhance mitochondrial biogenesis and leukemia progression.
5. Five novel SUCLG1 mutations in three Chinese patients with succinate-CoA ligase deficiency noticed b…

There were no clinical trials for SUCLG1;jsessionid=DE21CE054782BA308201C127F125EF1D;jsessionid=4A874CFD6189E76D087140613F0BC463;jsessionid=665276D51204178A15A093CF19B21511;jsessionid=FB0FBB4D83C400EFE20BCDF2677BBABD;jsessionid=6B09291086A036E5721463DE0E5F90AF