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

作者：Senwei Tan, Qiumeng Zhang, Rui Zhan, Luo Si, Yaoling Han, Bin Yu, Candace Muss, Véronique Pingault, Sandrine Marlin, Andrée Delahaye‐Duriez, Sophia Peters, Claudia Perne, Martina Kreiß, Nino Spataro, Juan Pablo Trujillo‐Quintero, Caroline Racine, Frédéric Tran Mau‐Them, Chanika Phornphutkul, Aaron D. Besterman, Julián A. Martínez-Agosto, Xiuxia Wang, Xiaoyu Tian, Siddharth Srivastava, David K. Urion, Jill A. Madden, Hind Al Saif, Michelle M. Morrow, Amber Begtrup, Xing Li, Sarah Jurgensmeyer, Peter Leahy, Shimin Zhou, Faxiang Li, Zhengmao Hu, Jieqiong Tan, Kun Xia, Hui Guo · 发表于：Molecular Psychiatry · 年份：2024 · DOI：10.1038/s41380-024-02806-z · 被引用次数：7 · 研究领域：Genomics and Rare Diseases、Genetics and Neurodevelopmental Disorders、Genetic Syndromes and Imprinting