Sodium channel SCN8A (Nav1.6): properties and de novo mutations in epileptic encephalopathy and intellectual disability

Overview of attention for article published in Frontiers in Genetics, January 2013

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SCN8A mutations - an emerging cause of epileptic encephalopathy & related phenotypes: http://t.co/5qJVMyhsbO

Sodium channel SCN8A (Nav1.6): properties and de novo mutations in epileptic encephalopathy a... http://t.co/P5IpByTr5A #genetics #genes

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