DOI:
10.1055/s-00000071
Seminars in Neurology
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References
Brautbar A, Wang J, Abdenur JE , et al.
The mitochondrial 13513G > A mutation is associated with Leigh disease phenotypes independent of complex I deficiency in muscle.
Mol Genet Metab 2008;
94 (4) 485-490
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