A novel hemizygous loss-of-function mutation in ADGRG2 causes male infertility with congenital bilateral absence of the vas deferens
Huan Wu(Ministry of Education of the People's Republic of China), Yunxia Cao(Anhui Medical University), Fuxi Zhu(Anhui Medical University), Mingrong Lv(Anhui Medical University), Cong Ma(Anhui Medical University), Nagwa Elshewy(Anhui Medical University), Xiaojin He(First Affiliated Hospital of Anhui Medical University), Shixiong Tian(Geological Exploration Technology Institute of Jiangsu Province), Zhaolian Wei(Anhui Medical University), Chunyu Liu(Jiamusi University), Jiajia Wang(Dalian Medical University), Feng Zhang(Affiliated Hospital of North Sichuan Medical College), Ping Zhou(Ministry of Education of the People's Republic of China), Xiaofeng Xu(Qingdao University), Xiaoqing Ni(Ministry of Education of the People's Republic of China), Huiru Cheng(Anhui Medical University), Qunshan Shen(Anhui Medical University), Qing Tan(Washington University in St. Louis), Yang Gao(Ministry of Education of the People's Republic of China)
Cited by 26
Related Papers
Genetic evidence supports demic diffusion of Han culture
|Nature|2004|482
Autism-like behaviours and germline transmission in transgenic monkeys overexpressing MeCP2
|Nature|2016|328
<i>TBX6</i> Null Variants and a Common Hypomorphic Allele in Congenital Scoliosis
|New England Journal of Medicine|2015|317
Bi-allelic DNAH8 Variants Lead to Multiple Morphological Abnormalities of the Sperm Flagella and Primary Male Infertility
|The American Journal of Human Genetics|2020|207