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Enhanced sensitivity of laforin- and malin-deficient mice to the convulsant agent pentylenetetrazole
Lafora disease is a rare form of inherited progressive myoclonus epilepsy caused by mutations in the EPM2A gene encoding laforin, or in the EPM2B gene, which encodes malin. It is characterized by the presence of polyglucosan inclusion bodies (Lafora bodies) in brain and other tissues. Genetically en...
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| Main Authors: | , , , |
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| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
Frontiers Media S.A.
2014
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| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4162417/ https://ncbi.nlm.nih.gov/pubmed/25309313 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fnins.2014.00291 |
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