4 Article(s)Download |
PMID | Title | Pub. Year | #Total Relationships |
1 | 33230181 | SUCLA2 mutations cause global protein succinylation contributing to the pathomechanism of a hereditary mitochondrial disease. | 2020 Nov 23 | 1 |
2 | 27913098 | Succinyl-CoA synthetase (SUCLA2) deficiency in two siblings with impaired activity of other mitochondrial oxidative enzymes in skeletal muscle without mitochondrial DNA depletion. | 2017 Mar | 1 |
3 | 25315394 | A comprehensive proteomic approach to identifying capacitation related proteins in boar spermatozoa. | 2014 Oct 14 | 1 |
4 | 17301081 | SUCLA2 mutations are associated with mild methylmalonic aciduria, Leigh-like encephalomyopathy, dystonia and deafness. | 2007 Mar | 2 |