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pro vyhledávání: '"Hamoud Khallaf"'
Publikováno v:
Brain Disorders, Vol 9, Iss , Pp 100070- (2023)
The GluN1 subunit of the N-methyl-d-aspartate (NMDA) receptor is encoded by GRIN1 gene. Mutations in this gene can cause neurodevelopmental disorders with or without hyperkinetic movements and seizures. It can be inherited as either autosomal dominan
Externí odkaz:
https://doaj.org/article/4380078fd35b458ba2f3d14be3374f2e
Publikováno v:
Brain Disorders. 9:100070