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Publikováno v:
Frontiers in Synaptic Neuroscience, Vol 14 (2023)
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 di
Externí odkaz:
https://doaj.org/article/a2e39ed0c7724de9a6e63e84c5db66b2