Pediatric Neurology Briefs (Jun 2015)
GRIN1 Mutations in Early-Onset Epileptic Encephalopathy
Abstract
Investigators from Yokohama City University and other medical centers in Israel and Japan reported mutations on N-methyl-D-aspartate (NMDA) receptors subunit GRIN1 (GluN1) identified in patients with nonsyndromic intellectual disability and early-onset epileptic encephalopathy.
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