![Dystonia and deafness due to SUCLA2 defect; Clinical course and biochemical markers in 16 children - ScienceDirect Dystonia and deafness due to SUCLA2 defect; Clinical course and biochemical markers in 16 children - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S156772490900124X-gr1.jpg)
Dystonia and deafness due to SUCLA2 defect; Clinical course and biochemical markers in 16 children - ScienceDirect
![Disorders caused by deficiency of succinate‐CoA ligase - Ostergaard - 2008 - Journal of Inherited Metabolic Disease - Wiley Online Library Disorders caused by deficiency of succinate‐CoA ligase - Ostergaard - 2008 - Journal of Inherited Metabolic Disease - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/8089a330-b937-4615-8582-d0120ea7f195/jimd0226-fig-0001-m.jpg)
Disorders caused by deficiency of succinate‐CoA ligase - Ostergaard - 2008 - Journal of Inherited Metabolic Disease - Wiley Online Library
![Succinyl-CoA ligase ADP-forming subunit beta promotes stress granule assembly to regulate redox and drive cancer metastasis | PNAS Succinyl-CoA ligase ADP-forming subunit beta promotes stress granule assembly to regulate redox and drive cancer metastasis | PNAS](https://www.pnas.org/cms/10.1073/pnas.2217332120/asset/4e180185-6960-4cff-9efc-dcd6509c256a/assets/images/large/pnas.2217332120fig03.jpg)
Succinyl-CoA ligase ADP-forming subunit beta promotes stress granule assembly to regulate redox and drive cancer metastasis | PNAS
![SUCLA2 mutations cause global protein succinylation contributing to the pathomechanism of a hereditary mitochondrial disease | Nature Communications SUCLA2 mutations cause global protein succinylation contributing to the pathomechanism of a hereditary mitochondrial disease | Nature Communications](https://media.springernature.com/lw685/springer-static/image/art%3A10.1038%2Fs41467-020-19743-4/MediaObjects/41467_2020_19743_Fig2_HTML.png)
SUCLA2 mutations cause global protein succinylation contributing to the pathomechanism of a hereditary mitochondrial disease | Nature Communications
![Succinyl-CoA ligase ADP-forming subunit beta promotes stress granule assembly to regulate redox and drive cancer metastasis | PNAS Succinyl-CoA ligase ADP-forming subunit beta promotes stress granule assembly to regulate redox and drive cancer metastasis | PNAS](https://www.pnas.org/cms/10.1073/pnas.2217332120/asset/ef9e5bda-77e3-4c9b-9706-b528e3d4c1fb/assets/images/large/pnas.2217332120fig07.jpg)
Succinyl-CoA ligase ADP-forming subunit beta promotes stress granule assembly to regulate redox and drive cancer metastasis | PNAS
Succinyl-CoA synthetase (SUCLA2) deficiency in two siblings with impaired activity of other mitochondrial oxidative enzymes in s
![Analysis of the effects of SUCLA2 missense mutations on the structure... | Download Scientific Diagram Analysis of the effects of SUCLA2 missense mutations on the structure... | Download Scientific Diagram](https://www.researchgate.net/publication/237199200/figure/fig1/AS:267578719338522@1440807146532/Analysis-of-the-effects-of-SUCLA2-missense-mutations-on-the-structure-of-encoded-protein.png)
Analysis of the effects of SUCLA2 missense mutations on the structure... | Download Scientific Diagram
![Figure 1 from SUCLA2 mutations are associated with mild methylmalonic aciduria, Leigh-like encephalomyopathy, dystonia and deafness. | Semantic Scholar Figure 1 from SUCLA2 mutations are associated with mild methylmalonic aciduria, Leigh-like encephalomyopathy, dystonia and deafness. | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/55fb829e195654ecaf54b29357b75ff261f94266/2-Figure1-1.png)
Figure 1 from SUCLA2 mutations are associated with mild methylmalonic aciduria, Leigh-like encephalomyopathy, dystonia and deafness. | Semantic Scholar
![SUCLA2 mutations cause global protein succinylation contributing to the pathomechanism of a hereditary mitochondrial disease | Nature Communications SUCLA2 mutations cause global protein succinylation contributing to the pathomechanism of a hereditary mitochondrial disease | Nature Communications](https://media.springernature.com/full/springer-static/image/art%3A10.1038%2Fs41467-020-19743-4/MediaObjects/41467_2020_19743_Fig1_HTML.png)
SUCLA2 mutations cause global protein succinylation contributing to the pathomechanism of a hereditary mitochondrial disease | Nature Communications
![SUCLA2-coupled regulation of GLS succinylation and activity counteracts oxidative stress in tumor cells - ScienceDirect SUCLA2-coupled regulation of GLS succinylation and activity counteracts oxidative stress in tumor cells - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S1097276521002690-gr7.jpg)