Back to matchesWe found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleNovel mutation in the NHLRC1 gene in a Malian family with a severe phenotype of Lafora disease.AuthorsTraoré, M.; Landouré, G.; Motley, W.; Sangaré, M.; Meilleur, K.; Coulibaly, S.; Traoré, S.; Niaré, B.; Mochel, F.; La Pean, A.; Vortmeyer, A.; Mani, H.; Fischbeck, K. H.PublicationNeurogenetics, 2009, Vol 10, Issue 4, p319ISSN1364-6745Publication typeArticleDOI10.1007/s10048-009-0190-4