A de novo missense mutation in MPP2 confers an increased risk of Vogt-Koyanagi-Harada disease as shown by trio-based whole-exome sequencing
三重全外显子组测序显示 MPP2 的新生错义突变会增加患 Vogt-Koyanagi-Harada 病的风险
期刊:Cellular & Molecular Immunology
影响因子:21.8
doi:10.1038/s41423-023-01088-9
Xianyang Liu #, Jiayu Meng #, Xingyun Liao #, Yusen Liu #, Qian Zhou, Zongren Xu, Shuming Yin, Qingfeng Cao, Guannan Su, Siyuan He, Wanqian Li, Xiaotang Wang, Guoqing Wang, Dali Li, Peizeng Yang, Shengping Hou