Associated Papers
Succinyl-CoA Synthetase Dysfunction as a Mechanism of Mitochondrial Encephalomyopathy: More than Just an Oxidative Energy Deficit.
Lancaster MS et al.
International Journal of Molecular Sciences, 2023
SUCLG1 mutations and mitochondrial encephalomyopathy: a case study and review of the literature.
Molaei Ramsheh S et al.
Molecular Biology Reports, 2020
[Phenotype and genotype of twelve Chinese children with mitochondrial DNA depletion syndromes].
Dai LF et al.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics, 2019
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