De novo monoallelic Reelin missense variants cause dominant neuronal migration disorders via a dominant-negative mechanism
从头发生的单等位基因Reelin错义变异通过显性负性机制导致显性神经元迁移障碍。
期刊:Journal of Clinical Investigation
影响因子:13.6
doi:10.1172/JCI153097
Riva, Martina; Ferreira, Sofia; Hayashi, Kotaro; Saillour, Yoann; Medvedeva, Vera P; Honda, Takao; Hayashi, Kanehiro; Altersitz, Claire; Albadri, Shahad; Rosello, Marion; Dang, Julie; Serafini, Malo; Causeret, Frédéric; Henry, Olivia J; Roux, Charles-Joris; Bellesme, Céline; Freri, Elena; Josifova, Dragana; Parrini, Elena; Guerrini, Renzo; Del Bene, Filippo; Nakajima, Kazunori; Bahi-Buisson, Nadia; Pierani, Alessandra