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Yildiz, E. et al. (2017). A novel EPM2A mutation in a patient with Lafora disease presenting with early parkinsonism symptoms in childhood. Seizure. pp. 77-79. [Online].
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Yildiz, E. et al. (2017). A novel EPM2A mutation in a patient with Lafora disease presenting with early parkinsonism symptoms in childhood. Seizure. pp. 77-79. [Online].