Clinical and molecular features of mitochondrial DNA depletion syndromes - Spinazzola - 2009 - Journal of Inherited Metabolic Disease - Wiley Online Library
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Screening of small molecules that selectively kill SUCLA2-deleted... | Download Scientific Diagram
SUCLA2 Polyclonal Antibody (PA5-118292)
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SUCLA2 mutations cause global protein succinylation contributing to the pathomechanism of a hereditary mitochondrial disease | Nature Communications
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IJMS | Free Full-Text | Succinyl-CoA Synthetase Dysfunction as a Mechanism of Mitochondrial Encephalomyopathy: More than Just an Oxidative Energy Deficit