Novel glycogen synthase kinase 3 and ubiquitination pathways in progressive myoclonus epilepsy

By Lohi Hannes  

Human Molecular Genetics, Vol. 14, Iss. 18, 2005-09 ,pp. : 2727-2736

Oxford University Press

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A novel protein tyrosine phosphatase gene is mutated in progressive myoclonus epilepsy of the Lafora type (EPM2)

By Topcu M.  

Human Molecular Genetics, Vol. 8, Iss. 2, 1999-02 ,pp. : 345-352

Oxford University Press

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Laforin preferentially binds the neurotoxic starch-like polyglucosans, which form in its absence in progressive myoclonus epilepsy

By Chan Elayne M.   Ackerley Cameron A.   Lohi Hannes   Ianzano Leonarda   Cortez Miguel A.   Shannon Patrick   Scherer Stephen W.   Minassian Berge A.  

Human Molecular Genetics, Vol. 13, Iss. 11, 2004-06 ,pp. : 1117-1129

Oxford University Press

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Laforin, defective in the progressive myoclonus epilepsy of Lafora type, is a dual-specificity phosphatase associated with polyribosomes

By Ganesh Subramaniam   Agarwala Kishan Lal   Ueda Kazunori  

Human Molecular Genetics, Vol. 9, Iss. 15, 2000-09 ,pp. : 2251-2261

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Modulation of functional properties of laforin phosphatase by alternative splicing reveals a novel mechanism for the EPM2A gene in Lafora progressive myoclonus epilepsy

By Dubey Deepti   Ganesh Subramaniam  

Human Molecular Genetics, Vol. 17, Iss. 19, 2008-10 ,pp. : 3010-3020

Oxford University Press

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