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Dystonia and deafness due to SUCLA2 defect; Clinical course and biochemical markers in 16 children - ScienceDirect
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Thymoquinone targets SUCLA2 loss that collaterally takes place with RB1... | Download Scientific Diagram
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Analysis of the effects of SUCLA2 missense mutations on the structure... | Download Scientific Diagram
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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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SUCLA2-coupled regulation of GLS succinylation and activity counteracts oxidative stress in tumor cells - 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
![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
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SUCLA2 Rabbit anti-Human, Mouse, Rat, Polyclonal, Proteintech 20 μL; Unconjugated products | Fisher Scientific
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PDF) SUCLA2 mutations are associated with mild methylmalonic aciduria, Leigh-like encephalomyopathy, dystonia and deafness
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