Bi-allelic variants in DNHD1 cause flagellar axoneme defects and asthenoteratozoospermia in humans and mice
DNHD1基因的双等位基因变异会导致人类和小鼠出现鞭毛轴丝缺陷和弱精子症。
期刊:American Journal of Human Genetics
影响因子:8.1
doi:10.1016/j.ajhg.2021.11.022
Chen Tan ,Lanlan Meng ,Mingrong Lv ,Xiaojin He ,Yanwei Sha ,Dongdong Tang ,Yaqi Tan ,Tongyao Hu ,Wenbin He ,Chaofeng Tu ,Hongchuan Nie ,Huan Zhang ,Juan Du ,Guangxiu Lu ,Li-Qing Fan ,Yunxia Cao ,Ge Lin ,Yue-Qiu Tan