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Progressive myoclonus epilepsy with polyglucosan bodies: Lafora disease.

Berge A Minassian

Journal: Advances in neurology 2002;89():199-210

PMID: 11968446

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Abstract

Address: Department of Pediatrics (Neurology), Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada.

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MeSH Terms: Brain, Diagnosis, Differential, Disease Progression, Glucans, Humans, Lafora Disease, Mutation, Protein Tyrosine Phosphatases, Protein Tyrosine Phosphatases, Non-Receptor, Spinal Cord
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