Pediatric Neurology Briefs (Jun 2015)

GRIN1 Mutations in Early-Onset Epileptic Encephalopathy

  • Wenjuan Chen,
  • Hongjie Yuan

DOI
https://doi.org/10.15844/pedneurbriefs-29-6-3
Journal volume & issue
Vol. 29, no. 6

Abstract

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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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