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GRIN2B-related neurodevelopmental disorder: current understanding of pathophysiological mechanisms

The GRIN2B-related neurodevelopmental disorder is a rare disease caused by mutations in the GRIN2B gene, which encodes the GluN2B subunit of NMDA receptors. Most individuals with GRIN2B-related neurodevelopmental disorder present with intellectual disability and developmental delay. Motor impairment...

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Hoofdauteurs: Shasta L. Sabo, Jessica M. Lahr, Madelyn Offer, Anika LA Weekes, Michael P. Sceniak
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: Frontiers Media S.A. 2023-01-01
Reeks:Frontiers in Synaptic Neuroscience
Onderwerpen:
GRIN2B
GluN2B (NMDA receptor subunit NR2B)
dendrite development
autism (ASD)
neuron development
disease variants
Online toegang:https://www.frontiersin.org/articles/10.3389/fnsyn.2022.1090865/full
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