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.

Keywords

• ndma receptors
• glun1
• epilepsy