δ-Catenin (CTNND2) missense mutation in familial cortical myoclonic tremor and epilepsy
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DOI: 10.1212/wnl.0000000000004709
Abstract: Objective: To identify the causative gene in a large Dutch family with familial cortical myoclonic tremor and epilepsy (FCMTE). Methods: We performed exome sequencing for 3 patients of our FCMTE family. Next, we performed knock-down… read more here.
Keywords: ctnnd2; myoclonic tremor; familial cortical; cortical myoclonic ... See more keywords