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SUCLG1
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SUCLG1 mutations and mitochondrial encephalomyopathy: a case study and review of the literature.
Expanding the phenotypic spectrum of Succinyl-CoA ligase deficiency through functional validation of…
Succinate-CoA ligase deficiency due to mutations in SUCLA2 and SUCLG1: phenotype and genotype correl…
SUCLG1 restricts POLRMT succinylation to enhance mitochondrial biogenesis and leukemia progression.
Five novel SUCLG1 mutations in three Chinese patients with succinate-CoA ligase deficiency noticed b…
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Deoxynucleosides Pyrimidines as Treatment for Mitochondrial Depletion Syndrome
Study to Evaluate Efficacy and Safety of Elamipretide in Subjects With Primary Mitochondrial Disease…
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