The unique evolution of the carbohydrate‐binding module CBM20 in laforin
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DOI: 10.1002/1873-3468.12994
Abstract: Laforin catalyses 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 module… read more here.
Keywords: cbm20 laforin; carbohydrate binding; binding module; laforin ... See more keywords