MARK2 variants cause autism spectrum disorder via the downregulation of WNT/β-catenin signaling pathway
Titel:
MARK2 variants cause autism spectrum disorder via the downregulation of WNT/β-catenin signaling pathway
Auteur:
Gong, Maolei Li, Jiayi Qin, Zailong Machado Bressan Wilke, Matheus Vernet Liu, Yijun Li, Qian Liu, Haoran Liang, Chen Morales-Rosado, Joel A. Cohen, Ana S.A. Hughes, Susan S. Sullivan, Bonnie R. Waddell, Valerie van den Boogaard, Marie-José H. van Jaarsveld, Richard H. van Binsbergen, Ellen van Gassen, Koen L. Wang, Tianyun Hiatt, Susan M. Amaral, Michelle D. Kelley, Whitley V. Zhao, Jianbo Feng, Weixing Ren, Changhong Yu, Yazhen Boczek, Nicole J. Ferber, Matthew J. Lahner, Carrie Elliott, Sherr Ruan, Yiyan Mignot, Cyril Keren, Boris Xie, Hua Wang, Xiaoyan Popp, Bernt Zweier, Christiane Piard, Juliette Coubes, Christine Mau-Them, Frederic Tran Safraou, Hana Innes, A. Micheil Gauthier, Julie Michaud, Jacques L. Koboldt, Daniel C. Sylvie, Odent Willems, Marjolaine Tan, Wen-Hann Cogne, Benjamin Rieubland, Claudine Braun, Dominique McLean, Scott Douglas Platzer, Konrad Zacher, Pia Oppermann, Henry Evenepoel, Lucie Blanc, Pierre El Khattabi, Laïla Haque, Neshatul Dsouza, Nikita R. Zimmermann, Michael T. Urrutia, Raul Klee, Eric W. Shen, Yiping Du, Hongzhen Rappaport, Leonard Liu, Chang-Mei Chen, Xiaoli