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	Title	Author(s)	Issue Date
	Pathogenic DDX3X Mutations Impair RNA Metabolism and Neurogenesis during Fetal Cortical Development Journal:Neuron	Lennox, AL Hoye, ML Jiang, R Johnson-Kerner, BL Suit, LA Venkataramanan, S Sheehan, CJ Alsina, FC Fregeau, B Aldinger, KA Moey, C Lobach, I Afenjar, A Babovic-Vuksanovic, D Bezieau, S Blackburn, PR Bunt, J Burglen, L Campeau, PM Charles, P Chung, BHY Cogne, B Curry, C D'Agostino, MD Di Donato, N Faivre, L Heron, D Innes, AM Isidor, B Keren, B Kimball, A Klee, EW Kuentz, P Kury, S Martin-Coignard, D Mirzaa, G Mignot, C Myake, N Matsumoto, N Fujita, A Nava, C Nizon, M Rodriguez, D Blok, LS Thauvin-Robinet, C Thevenon, J Vincent, M Ziegler, A Dobyns, W Richards, LJ Barkovich, AJ Floor, SN Silver, DL Sherr, EH	2020
	Recurrent de novo missense variants in GNB2 can cause syndromic intellectual disability Journal:Journal of Medical Genetics	Tan, NB Pagnamenta, AT Ferla, MP Gadian, J Chung, BHY Chan, MCY Fung, LF Cook, E Guter, S Boschann, F Heinen, A Schallne, J Mignot, C Keren, B Whalen, S Sarret, C Mittag, D Demmer, L Stapleton, R Saida, K Matsumoto, N Miyake, N Sheffer, R Mor-Shaked, H Barnett, CP Byrne, AB Scott, HS Kraus, A Cappuccio, G Brunetti-Pierri, N Iorio, R Di Dato, F Pais, LS Yeung, A Tan, TY Taylor, JC Christodoulou, J White, S	2021
	The epileptology of GNB5 encephalopathy Journal:Epilepsia	Poke, G King, C Muir, A de Valles-Ibariez, G Germano, M Moura de Souza, CF Fung, J Chung, B Fung, CW Mignot, C Ilea, A Keren, B Vermersch, AI Davis, S Stanley, T Moharir, M Kannu, P Shao, Z Malerba, N Merla, G Mefford, HC Scheffer, IE Sadleir, LG	2019

Showing results 1 to 3 of 3