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Neurology|March 29, 2007
Genetic diagnosis in Lafora disease: genotype-phenotype correlations and diagnostic pitfallsH Lohi, J Turnbull, X C Zhao, et al.Annals of Neurology|April 18, 1998
Angelman syndrome: correlations between epilepsy phenotypes and genotypesB A Minassian, T M DeLorey, R W Olsen, et al.Journal of Medical Genetics|September 10, 2003
Genetic mapping of a new Lafora progressive myoclonus epilepsy locus (EPM2B) on 6p22E M Chan, D E Bulman, A D Paterson, et al.The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|October 8, 1998
Mice lacking the beta3 subunit of the GABAA receptor have the epilepsy phenotype and many of the behavioral characteristics of Angelman syndromeT M DeLorey, A Handforth, S G Anagnostaras, et al.Annals of Neurology|February 16, 1999
Genetic locus heterogeneity in Lafora's progressive myoclonus epilepsyB A Minassian, J Sainz, J M Serratosa, et al.Nature Genetics|October 15, 1998
Mutations in a gene encoding a novel protein tyrosine phosphatase cause progressive myoclonus epilepsyB A Minassian, J R Lee, J A Herbrick, et al.Pageof 3