DOI:
10.1055/s-00000071
Seminars in Neurology
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References
Randolph LM, Jackson HA, Wang J , et al.
Fatal infantile lactic acidosis and a novel homozygous mutation in the SUCLG1 gene: a mitochondrial DNA depletion disorder.
Mol Genet Metab 2011;
102 (2) 149-152
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