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The unique evolution of the carbohydrate-binding module CBM20 in laforin
Laforin catalyzes glycogen dephosphorylation. Mutations in its gene result in Lafora disease, a fatal progressive myoclonus epilepsy, the hallmark being water-insoluble, hyperphosphorylated carbohydrate inclusions called Lafora bodies. Human laforin consists of an N-terminal carbohydrate-binding mod...
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| Publicado no: | FEBS Lett |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5829021/ https://ncbi.nlm.nih.gov/pubmed/29389008 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/1873-3468.12994 |
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