Mutations in a gene encoding a novel protein tyrosine phosphatase cause progressive myoclonus epilepsy

Berge A. Minassian, R. Lee Jeffrey, Jo Anne Herbrick, Jack Huizenga, Sylvia Soder, Andrew J. Mungall, Ian Dunham, Rebecca Gardner, Chung Yan G. Fong, Stirling Carpenter, Laura Jardim, P. Satishchandra, Eva Andermann, O. Carter Snead, Iscia Lopes-Cendes, Lap Chee Tsui, Antonio V. Delgado-Escueta, Guy A. Rouleau, Stephen W. Scherer

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Lafora's disease (LD; OMIM 254780) is an autosomal recessive form of progressive myoclonus epilepsy characterized by seizures and cumulative neurological deterioration. Onset occurs during late childhood and usually results in death within ten years of the first symptoms1,2. With few exceptions, patients follow a homogeneous clinical course despite the existence of genetic heterogeneity3. Biopsy of various tissues, including brain, revealed characteristic polyglucosan inclusions called Lafora bodies4-8, which suggested LD might be a generalized storage disease6,9. Using a positional cloning approach, we have identified at chromosome 6q24 a novel gene, EPM2A, that encodes a protein with consensus amino acid sequence indicative of a protein tyrosine phosphatase (PTP). mRNA transcripts representing alternatively spliced forms of EPM2A were found in every tissue examined, including brain. Six distinct DNA sequence variations in EPM2A in nine families, and one homozygous microdeletion in another family, have been found to cosegregate with LD. These mutations are predicted to cause deleterious effects in the putative protein product, named laforin, resulting in LD.

Original languageEnglish (US)
Pages (from-to)171-174
Number of pages4
JournalNature genetics
Issue number2
StatePublished - Oct 15 1998


ASJC Scopus subject areas

  • Genetics

Cite this

Minassian, B. A., Lee Jeffrey, R., Herbrick, J. A., Huizenga, J., Soder, S., Mungall, A. J., Dunham, I., Gardner, R., Fong, C. Y. G., Carpenter, S., Jardim, L., Satishchandra, P., Andermann, E., Carter Snead, O., Lopes-Cendes, I., Tsui, L. C., Delgado-Escueta, A. V., Rouleau, G. A., & Scherer, S. W. (1998). Mutations in a gene encoding a novel protein tyrosine phosphatase cause progressive myoclonus epilepsy. Nature genetics, 20(2), 171-174.