GRIN1 Mutations in Early-Onset Epileptic Encephalopathy
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.
| Main Authors: | , |
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| Format: | Article |
| Language: | English |
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Pediatric Neurology Briefs Publishers
2015-06-01
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| Series: | Pediatric Neurology Briefs |
| Subjects: | |
| Online Access: | https://www.pediatricneurologybriefs.com/articles/95 |