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Nature Genetics, ISSN 1061-4036, 01/2015, Volume 47, Issue 1, pp. 39 - 46
Journal Article
ORPHANET JOURNAL OF RARE DISEASES, ISSN 1750-1172, 06/2019, Volume 14, Issue 1, pp. 149 - 149
BackgroundLafora disease (LD) is a rare, lethal, progressive myoclonus epilepsy for which no targeted therapy is currently available. Studies on a mouse model... 
EPM2A | MEDICINE, RESEARCH & EXPERIMENTAL | EPM2B | ACTIVATED PROTEIN-KINASE | GENETICS & HEREDITY | Progressive myoclonus epilepsy | NHLRC1 | Metformin | MODEL | Lafora disease | Nervous system diseases | Dosage and administration | Genetic aspects | Drug therapy
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 06/2012, Volume 90, Issue 6, pp. 1102 - 1107
Journal Article
Annals of Neurology, ISSN 0364-5134, 05/2017, Volume 81, Issue 5, pp. 677 - 689
Journal Article
Human Genetics, ISSN 0340-6717, 10/2016, Volume 135, Issue 10, pp. 1117 - 1125
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 05/2011, Volume 88, Issue 5, pp. 566 - 573
Journal Article