QuickView for Galpha;jsessionid=3E7B2B1D5DC375C1F105CC1855F3A17F;jsessionid=627D7225BDAEA17424B0FAFF2202B4F9;jsessionid=E68BCBD791A2F89F23271BC7393DA1DC (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. Five novel SUCLG1 mutations in three Chinese patients with succinate-CoA ligase deficiency noticed b…
5. A SUCLG1 mutation in a patient with mitochondrial DNA depletion and congenital anomalies.

There were no clinical trials for Galpha;jsessionid=3E7B2B1D5DC375C1F105CC1855F3A17F;jsessionid=627D7225BDAEA17424B0FAFF2202B4F9;jsessionid=E68BCBD791A2F89F23271BC7393DA1DC