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Pediatric Neurology Briefs: Volume 29, Issue 06

GRIN1 Mutations in Early-Onset Epileptic Encephalopathy Open Access (recommended)

Descriptions

Resource type(s)
Article
Keyword
Epilepsy
GluN1
NDMA receptors
Rights
Attribution 4.0 International

Creator
Chen, Wenjuan
Yuan, Hongjie
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.
Publisher
DigitalHub. Galter Health Sciences Library
Pediatric Neurology Briefs Publishers
Date Created
2015
Original Identifier
PNB-29-44
Language
English
Subject: MESH
Neurosurgery
Pediatrics
Child Development
Child
Neurology
Nervous System Diseases
Infant
Brain Diseases
DOI
10.15844/pedneurbriefs-29-6-3

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Mime type: application/pdf
File size: 147.3 kB