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Monoallelic loss-of-function variants in GSK3B lead to autism and developmental delay

Title:	Monoallelic loss-of-function variants in GSK3B lead to autism and developmental delay
Authors:	Tan, Senwei^Aff1; Zhang, Qiumeng^Aff1; Zhan, Rui^Aff1; Luo, Si^Aff1; Han, Yaoling^Aff1; Yu, Bin^Aff1; Muss, Candace^Aff2; Pingault, Veronique^Aff3; Marlin, Sandrine^{Aff4, Aff5}; Delahaye, Andrée^Aff3; Peters, Sophia^Aff6; Perne, Claudia^Aff6; Kreiß, Martina^Aff6; Spataro, Nino^Aff7; Trujillo-Quintero, Juan Pablo^Aff7; Racine, Caroline^Aff8; Tran-Mau-Them, Frederic^Aff8; Phornphutkul, Chanika^Aff9; Besterman, Aaron D.^{Aff10, Aff11, Aff12}; Martinez, Julian^Aff13; Wang, Xiuxia^Aff14; Tian, Xiaoyu^Aff14; Srivastava, Siddharth^Aff15; Urion, David K.^Aff15; Madden, Jill A.^{Aff16, Aff17}; Saif, Hind Al^Aff18; Morrow, Michelle M.^Aff19; Begtrup, Amber^Aff19; Li, Xing^Aff20; Jurgensmeyer, Sarah^{Aff21, Aff22}; Leahy, Peter^{Aff21, Aff22}; Zhou, Shimin^Aff1; Li, Faxiang^Aff1; Hu, Zhengmao^Aff1; Tan, Jieqiong^Aff1; Xia, Kun^{Aff1, Aff23, Aff24, IDs4138002402806z_cor1}; Guo, Hui^{Aff1, Aff24, IDs4138002402806z_cor2}
Source:	Molecular Psychiatry. 30(5):1952-1965
Database:	Springer Nature Journals