Cranial MRI of MDS. Cranial MRI of the patient with SUCLA2 mutation... | Download Scientific Diagram
SUCLA2 mutations cause global protein succinylation contributing to the pathomechanism of a hereditary mitochondrial disease | Nature Communications
Clinical and molecular features of mitochondrial DNA depletion syndromes - Spinazzola - 2009 - Journal of Inherited Metabolic Disease - Wiley Online Library
The GABA Transaminase, ABAT, Is Essential for Mitochondrial Nucleoside Metabolism
SUCLA2 mutations cause global protein succinylation contributing to the pathomechanism of a hereditary mitochondrial disease | Nature Communications