Mutations in SUCLA2: a tandem ride back to the Krebs cycle
Author:
Publisher
Oxford University Press (OUP)
Subject
Clinical Neurology
Link
http://academic.oup.com/brain/article-pdf/130/3/606/17343430/awm023.pdf
Reference30 articles.
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2. SUCLA2 mutations cause mild methylmalonic aciduria, Leigh-like encephalomyopathy, dystonia and deafness;Carrozzo;Brain,2007
3. Mutant mitochondrial elongation factor G1 and combined oxidative phosphorylation deficiency;Coenen;N Engl J Med,2004
4. Deficiency of the ADP-forming succinyl-CoA synthase activity is associated with encephalomyopathy and mitochondrial DNA depletion;Elpeleg;Am J Hum Genet,2005
5. Infantile hepatocerebral syndromes associated with mutations in the mitochondrial DNA polymerase-gammaA;Ferrari;Brain,2005
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