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Neurology|February 15, 2001
Atypical MELAS syndrome associated with a new mitochondrial tRNA glutamine point mutationM Bataillard, E Chatzoglou, L Rumbach, et al.
Journal of Inherited Metabolic Disease|April 17, 2008
L-2-hydroxyglutaric aciduria: identification of ten novel mutations in the L2HGDH geneJ O Sass, F Jobard, M Topçu, et al.
Neurology|April 29, 2011
CSF biomarkers in posterior cortical atrophyJ Seguin, M Formaglio, A Perret-Liaudet, et al.
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