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sucla2 protein human
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SUCLA2 Arg407Trp mutation can cause a nonprogressive movement disorder - deafness syndrome.
SUCLA2 mutations cause global protein succinylation contributing to the pathomechanism of a heredita…
SUCLA2-coupled regulation of GLS succinylation and activity counteracts oxidative stress in tumor ce…
Pharmacologically targetable vulnerability in prostate cancer carrying RB1-SUCLA2 deletion.
A Novel SUCLA2 Mutation Presenting as a Complex Childhood Movement Disorder.
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Deoxynucleosides Pyrimidines as Treatment for Mitochondrial Depletion Syndrome
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