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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Bibliografiske detaljer
Main Authors: DePaoli-Roach, Anna A., Segvich, Dyann M., Meyer, Catalina M., Rahimi, Yasmeen, Worby, Carolyn A., Gentry, Matthew S., Roach, Peter J.
Format: Artigo
Sprog:Inglês
Udgivet: Oxford University Press 2012
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Articles
Online adgang: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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