GRIN1 Mutations in Early-Onset Epileptic Encephalopathy

• मुख्य लेखकों: Wenjuan Chen (लेखक), Hongjie Yuan (लेखक)
• स्वरूप: पुस्तक
• प्रकाशित: Pediatric Neurology Briefs Publishers, 2015-06-01T00:00:00Z.
• विषय: article
• ऑनलाइन पहुंच: Connect to this object online.

Investigators from Yokohama City University and other medical centers in Israel and Japan reported mutations on N-methyl-D-aspartate (NMDA) receptors subunit <em>GRIN1</em> (GluN1) identified in patients with nonsyndromic intellectual disability and early-onset epileptic encephalopathy.