| 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 |