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Genetic mapping of a new Lafora progressive myoclonus epilepsy locus (EPM2B) on 6p22
Background: Lafora disease is a progressive myoclonus epilepsy with polyglucosan accumulations and a peculiar neurodegeneration with generalised organellar disintegration. It causes severe seizures, leading to dementia and eventually death in early adulthood. Methods: One Lafora disease gene, EPM2A,...
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| Hauptverfasser: | , , , , , , , , , |
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| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
BMJ Group
2003
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1735578/ https://ncbi.nlm.nih.gov/pubmed/12960212 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmg.40.9.671 |
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