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Article

A novel EPM2A mutation in a patient with Lafora disease presenting with early parkinsonism symptoms in childhood.

Seizure - 1 Oct 2017

Yildiz Edibe Pembegul, Yesil Gozde, Ozkan Melis Ulak, Bektas Gonca, Caliskan Mine, Ozmen Meral

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Share to Adolescent
Share to Cognitive Dysfunction
Share to Drug Resistant Epilepsy
Share to Lafora Disease

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Protein Tyrosine Phosphatases, Non-Receptor

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Identifiers

PMID: 28818698
DOI: 10.1016/j.seizure.2017.07.011

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