Regional and Developmental Expression of Epm2a Gene and Its Evolutionary Conservation

This publication has 15 references indexed in Scilit:

• Mutational spectrum of the EPM2A gene in progressive myoclonus epilepsy of Lafora: high degree of allelic heterogeneity and prevalence of deletions
  European Journal of Human Genetics, 2000
• Laforin, defective in the progressive myoclonus epilepsy of Lafora type, is a dual-specificity phosphatase associated with polyribosomes
  Human Molecular Genetics, 2000
• Mutation spectrum and predicted function of laforin in Lafora’s progressive myoclonus epilepsy
  Neurology, 2000
• Charcot-Marie-Tooth type 4B is caused by mutations in the gene encoding myotubularin-related protein-2
  Nature Genetics, 2000
• Identification of new and common mutations in the EPM2A gene in Lafora disease
  Neurology, 2000
• Isolation and Characterization of Mouse Homologue for the Human Epilepsy Gene,EPM2A
  Biochemical and Biophysical Research Communications, 1999
• A novel protein tyrosine phosphatase gene is mutated in progressive myoclonus epilepsy of the Lafora type (EPM2)
  Human Molecular Genetics, 1999
• Protein tyrosine phosphatases: counting the trees in the forest
  Gene, 1998
• Mutations in a gene encoding a novel protein tyrosine phosphatase cause progressive myoclonus epilepsy
  Nature Genetics, 1998
• A gene mutated in X–linked myotubular myopathy defines a new putative tyrosine phosphatase family conserved in yeast
  Nature Genetics, 1996