QuickView for Galpha;jsessionid=3E7B2B1D5DC375C1F105CC1855F3A17F;jsessionid=A06DB376F7D26A5D168C1C2BF963ABA7;jsessionid=817AF5180BA1C7B3D8EA126D15D39B5C;jsessionid=C79D327213F84D84F7D45FAD33A13A3F;jsessionid=A4CF5AE41571F5DF236EFDBE7A89E42C (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=A06DB376F7D26A5D168C1C2BF963ABA7;jsessionid=817AF5180BA1C7B3D8EA126D15D39B5C;jsessionid=C79D327213F84D84F7D45FAD33A13A3F;jsessionid=A4CF5AE41571F5DF236EFDBE7A89E42C