Laforin, a dual specificity protein phosphatase involved in Lafora disease, is phosphorylated at Ser25 by AMP-activated protein kinase

Lafora progressive myoclonus epilepsy (Lafora disease; LD) is a fatal autosomal recessive neurodegenerative disorder caused by loss-of-function mutations in either the EPM2A gene, encoding the dual specificity phosphatase laforin, or the EPM2B gene, encoding the E3-ubiquitin ligase malin. Previously...

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Bibliografische gegevens
Hoofdauteurs: Romá-Mateo, Carlos, Solaz-Fuster, Maria del Carmen, Gimeno-Alcañiz, José Vicente, Dukhande, Vikas V., Donderis, Jordi, Marina, Alberto, Criado, Olga, Koller, Antonius, de Cordoba, Santiago Rodriguez, Gentry, Matthew S., Sanz, Pascual
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: 2011
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Article
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC3299407/
https://ncbi.nlm.nih.gov/pubmed/21728993
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1042/BJ20110150
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