DOI:
10.1055/s-00029030
Journal of Pediatric Neurology
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References
Haudry C, de Lonlay P, Malan V. et al.
Maternal uniparental disomy of chromosome 2 in a patient with a DGUOK mutation associated with hepatocerebral mitochondrial DNA depletion syndrome.
Mol Genet Metab 2012;
107 (04) 700-704
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