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Common synaptic phenotypes arising from diverse mutations in the human NMDA receptor subunit GluN2A.
Autor:
Elmasri, Marwa1 (AUTHOR), Hunter, Daniel William1 (AUTHOR), Winchester, Giles1 (AUTHOR), Bates, Ella Emine1 (AUTHOR), Aziz, Wajeeha1 (AUTHOR), Van Der Does, Does Moolenaar1 (AUTHOR), Karachaliou, Eirini1 (AUTHOR), Sakimura, Kenji2 (AUTHOR), Penn, Andrew. Charles1 (AUTHOR) A.C.Penn@sussex.ac.uk
Publikováno v:
Communications Biology. 3/28/2022, Vol. 5 Issue 1, p1-17. 17p.