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Paper Details

SUCLA2 mutations cause global protein succinylation contributing to the pathomechanism of a hereditary mitochondrial disease.
Nat Commun
32
2020
(NAD+, (NAD+)-dependent desuccinylase, SCL, SCL deficiency, SIRT5, SUCLA2, Succinyl-CoA, Succinyl-CoA ligase, Succinyl-CoA ligase (SCL) deficiency, TCA, acyl-coenzyme A, hereditary mitochondrial disease, mitochondrial encephalomyopathy, myotubes, patient, patient-derived fibroblasts, patients, succinyl, succinyl-CoA, succinyl-CoA ligase subunit-, tricarboxylic acid, tricarboxylic acid cycle (TCA) gene, zebrafish
Author NameAffiliation
Jesse G MeyerBuck Institute for Research on Aging
Jesse G MeyerMedical College of Wisconsin
Jason W LocasaleDuke University School of Medicine
Birgit SchillingBuck Institute for Research on Aging
Birgit SchillingBuck Institute for Research on Aging
Eric VerdinGladstone Institutes and University of California san francisco
Eric VerdinBuck Institute for Research on Aging
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