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Glycogen metabolism in tissues from a mouse model of Lafora disease

Laforin, encoded by the EPM2A gene, by sequence is a member of the dual specificity protein phosphatase family. Mutations in the EPM2A gene account for around half of the cases of Lafora disease, an autosomal recessive neurodegenerative disorder, characterized by progressive myoclonus epilepsy. The...

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Detalhes bibliográficos
Main Authors: Wang, Wei, Lohi, Hannes, Skurat, Alexander V., DePaoli-Roach, Anna A., Minassian, Berge A., Roach, Peter J.
Formato: Artigo
Idioma:Inglês
Publicado em: 2006
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2577384/
https://ncbi.nlm.nih.gov/pubmed/17118331
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.abb.2006.10.017
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