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Paper Details

Functional analysis of a de novo GRIN2A missense mutation associated with early-onset epileptic encephalopathy.
Nat Commun
104
2014
GRIN2A, GluN2A, L812M, NMDA, NMDA receptors, NMDAR, NMDAR subunits, NMDARs, amino acid, cerebral atrophy, developmental delay, epilepsy, epileptic, epileptic encephalopathy, magnesium, neurological disorders, neuronal hyperexcitability, patient, protons, transmembrane, zinc
Author NameAffiliation
Thomas C MarkelloNational Institutes of Health, and National Human Genome Research Institute
Gretchen GolasNational Institutes of Health, and National Human Genome Research Institute
David R AdamsNational Institutes of Health, and National Human Genome Research Institute
David R AdamsNational Institutes of Health, and National Human Genome Research Institute
Cornelius F BoerkoelNational Institutes of Health, and National Human Genome Research Institute
Cornelius F BoerkoelNational Institutes of Health, and National Human Genome Research Institute
William A GahlNational Institutes of Health, and National Human Genome Research Institute
William A GahlNational Institutes of Health, and National Human Genome Research Institute
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