Story of a genetic shape-shifter: SCN2A in benign seizures, autism and epileptic encephalopathy
Beyond the Ion Channel,
The other sodium channel gene. The week before Christmas, the Kiel group identified its first patient with SCN2A encephalopathy.
Whole genome sequencing identifies SCN2A mutation in monozygotic twins with Ohtahara syndrome and unique neuropathologic findings
Overview of attention for article published in Epilepsia, March 2013
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