QuickView for SUCLG1;jsessionid=DE21CE054782BA308201C127F125EF1D;jsessionid=C10E58F5000BAC620B6CD7F510D1F0B5;jsessionid=2022AFF95DE1478179948CB4CDD5514E;jsessionid=1776A37B7D506B3F19745881025413A2 (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=C10E58F5000BAC620B6CD7F510D1F0B5;jsessionid=2022AFF95DE1478179948CB4CDD5514E;jsessionid=1776A37B7D506B3F19745881025413A2