GRIN1 Mutations in Early-Onset Epileptic Encephalopathy

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.

Bibliographic Details
Main Authors: Wenjuan Chen, Hongjie Yuan
Format: Article
Language:English
Published: Pediatric Neurology Briefs Publishers 2015-06-01
Series:Pediatric Neurology Briefs
Subjects:
ndma receptors
glun1
epilepsy
Online Access:https://www.pediatricneurologybriefs.com/articles/95
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spelling doaj-20abfb89b96a4dee98468b1e709ed9022020-11-25T02:15:42ZengPediatric Neurology Briefs PublishersPediatric Neurology Briefs1043-31552166-64822015-06-0129610.15844/pedneurbriefs-29-6-381GRIN1 Mutations in Early-Onset Epileptic EncephalopathyWenjuan Chen0Hongjie Yuan1Department of Pharmacology, Emory University, Atlanta, GADepartment of Pharmacology, Emory University, Atlanta, GAInvestigators 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.https://www.pediatricneurologybriefs.com/articles/95ndma receptorsglun1epilepsy
collection DOAJ
language English
format Article
sources DOAJ
author Wenjuan Chen
Hongjie Yuan
spellingShingle Wenjuan Chen
Hongjie Yuan
GRIN1 Mutations in Early-Onset Epileptic Encephalopathy
Pediatric Neurology Briefs
ndma receptors
glun1
epilepsy
author_facet Wenjuan Chen
Hongjie Yuan
author_sort Wenjuan Chen
title GRIN1 Mutations in Early-Onset Epileptic Encephalopathy
title_short GRIN1 Mutations in Early-Onset Epileptic Encephalopathy
title_full GRIN1 Mutations in Early-Onset Epileptic Encephalopathy
title_fullStr GRIN1 Mutations in Early-Onset Epileptic Encephalopathy
title_full_unstemmed GRIN1 Mutations in Early-Onset Epileptic Encephalopathy
title_sort grin1 mutations in early-onset epileptic encephalopathy
publisher Pediatric Neurology Briefs Publishers
series Pediatric Neurology Briefs
issn 1043-3155
2166-6482
publishDate 2015-06-01
description 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.
topic ndma receptors
glun1
epilepsy
url https://www.pediatricneurologybriefs.com/articles/95
work_keys_str_mv AT wenjuanchen grin1mutationsinearlyonsetepilepticencephalopathy
AT hongjieyuan grin1mutationsinearlyonsetepilepticencephalopathy
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