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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Detalles Bibliográficos
Autores principales: Sabo, Shasta L., Lahr, Jessica M., Offer, Madelyn, Weekes, Anika LA, Sceniak, Michael P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Neuroscience
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9873235/
https://www.ncbi.nlm.nih.gov/pubmed/36704660
http://dx.doi.org/10.3389/fnsyn.2022.1090865

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9873235/
https://www.ncbi.nlm.nih.gov/pubmed/36704660
http://dx.doi.org/10.3389/fnsyn.2022.1090865

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