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Laforin and malin knockout mice have normal glucose disposal and insulin sensitivity
Lafora disease is a fatal, progressive myoclonus epilepsy caused in ∼90% of cases by mutations in the EPM2A or EPM2B genes. Characteristic of the disease is the formation of Lafora bodies, insoluble deposits containing abnormal glycogen-like material in many tissues, including neurons, muscle, heart...
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| Autors principals: | , , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Oxford University Press
2012
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3298283/ https://ncbi.nlm.nih.gov/pubmed/22186021 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddr598 |
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