학술논문
YWHAE loss of function causes a rare neurodevelopmental disease with brain abnormalities in human and mouse
Document Type
Article
Author
Denommé-Pichon, A.-S.; Bruel, A.-L.; Chevarin, M.; Overs, A.; Vitobello, A.; Duffourd, Y.; Thauvin-Robinet, C.; Philippe, C.; Collins, S.C.; Thomas, Q.; Weber, M.; Faivre, L.; Yalcin, B.; Palomares-Bralo, M.; Santos-Simarro, F.; Mikhaleva, A.; Wagner, C.; Vancollie, V.E.; Lelliott, C.J.; Prada, C.E.; Pacio-Míguez, M.; Busa, T.; Legius, E.; Bacino, C.A.; Rosenfeld, J.A.; Le Guyader, G.; Egloff, M.; Le Guillou, X.; Mencarelli, M.A.; Renieri, A.; Grosso, S.; Levy, J.; Dozières, B.; Desguerre, I.
Source
In: Genetics in Medicine . (Genetics in Medicine, July 2023, 25(7))
Subject
Language
English
ISSN
15300366
10983600
10983600