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Identification of a novel protein interacting with laforin, the epm2a progressive myoclonus epilepsy gene product

✍ Scribed by Leonarda Ianzano; Xiao C Zhao; Berge A Minassian; Stephen W Scherer


Book ID
117592283
Publisher
Elsevier Science
Year
2003
Tongue
English
Weight
446 KB
Volume
81
Category
Article
ISSN
0888-7543

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Loss of function of the cytoplasmic isof
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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