학술논문
Missense variants in RPH3A cause defects in excitatory synaptic function and are associated with a clinically variable neurodevelopmental disorder
Document Type
Article
Author
Pavinato, L.; Brusco, A.; Stanic, J.; Barzasi, M.; Eberini, I.; Palazzolo, L.; Di Luca, M.; Gardoni, F.; Gurgone, A.; Chiantia, G.; Giustetto, M.; Cipriani, V.; Vestito, L.; Smedley, D.; Costa, A.; Marcantoni, A.; Biamino, E.; Spada, M.; Hiatt, S.M.; Kelley, W.V.; Sisodiya, S.M.; Efthymiou, S.; Chand, P.; Kaiyrzhanov, R.; Bruselles, A.; Cardaropoli, S.; Tartaglia, M.; De Rubeis, S.; Buxbaum, J.D.; Ferrero, G.B.
Source
In: Genetics in Medicine . (Genetics in Medicine, November 2023, 25(11))
Subject
Language
English
ISSN
15300366
10983600
10983600