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YWHAE loss of function causes a rare neurodevelopmental dis..:
Denommé-Pichon, Anne-Sophie
;
Collins, Stephan, C
;
Bruel, Ange-Line
...
info:eu-repo/semantics/altIdentifier/doi/10.1016/j.gim.2023.100835. , 2023
Link:
https://inserm.hal.science/inserm-04094776
RT Journal T1
YWHAE loss of function causes a rare neurodevelopmental disease with brain abnormalities in human and mouse
UL https://suche.suub.uni-bremen.de/peid=base-ftccsdartic:oai:HAL:inserm-04094776v1&Exemplar=1&LAN=DE A1 Denommé-Pichon, Anne-Sophie A1 Collins, Stephan, C A1 Bruel, Ange-Line A1 Mikhaleva, Anna A1 Wagner, Christel A1 Vancollie, Valerie, E A1 Thomas, Quentin A1 Chevarin, Martin A1 Weber, Mathys A1 Prada, Carlos, E A1 Overs, Alexis A1 Palomares-Bralo, María A1 Santos-Simarro, Fernando A1 Pacio-Míguez, Marta A1 Busa, Tiffany A1 Legius, Eric A1 Bacino, Carlos, A A1 Rosenfeld, Jill, A A1 Le Guyader, Gwenaël A1 Egloff, Matthieu A1 Le Guillou, Xavier A1 Mencarelli, Maria, Antonietta A1 Renieri, Alessandra A1 Grosso, Salvatore A1 Levy, Jonathan A1 Dozières, Blandine A1 Desguerre, Isabelle A1 Vitobello, Antonio A1 Duffourd, Yannis A1 Lelliott, Christopher, J A1 Thauvin-Robinet, Christel A1 Philippe, Christophe A1 Faivre, Laurence A1 Yalcin, Binnaz PB HAL CCSD; Nature Publishing Group YR 2023 K1 14-3-3 K1 Miller-Dieker syndrome K1 Neurodevelopmental disorders K1 YWHAE K1 brain abnormalities K1 knockout mouse model K1 [SDV]Life Sciences [q-bio] JF info:eu-repo/semantics/altIdentifier/doi/10.1016/j.gim.2023.100835 LK http://dx.doi.org/https://inserm.hal.science/inserm-04094776 DO https://inserm.hal.science/inserm-04094776 SF ELIB - SuUB Bremen
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