The Brown-Vialetto-Van Laere and Fazio Londe syndrome revisited: natural history, genetics, treatment and future perspectives

Cited by papers we hold 2

• Clinical and genetical heterogeneity of late-onset multiple acyl-coenzyme A dehydrogenase deficiency · 2014
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• Treatable childhood neuronopathy caused by mutations in riboflavin transporter RFVT2 · 2013
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