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Mutation spectrum and predicted function of laforin in Lafora's progressive myoclonus epilepsy

✍ Scribed by Minassian, B. A.; Ianzano, L.; Meloche, M.; Andermann, E.; Rouleau, G. A.; Delgado-Escueta, A. V.; Scherer, S. W.


Book ID
127193573
Publisher
Lippincott Williams and Wilkins
Year
2000
Tongue
English
Weight
239 KB
Volume
55
Category
Article
ISSN
0028-3878

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## Communicated by Stylianos Antonarakis Lafora disease is the most severe teenage-onset progressive epilepsy, a unique form of glycogenosis with perikaryal accumulation of an abnormal form of glycogen, and a neurodegenerative disorder exhibiting an unusual generalized organellar disintegration. Th