Novel mutations in LHCGR (luteinizing hormone/choriogonadotropin receptor): expanding the spectrum of mutations responsible for human empty follicle syndrome.
Zhihua ZhangLing WuFeiyang DiaoBiaobang ChenJing FuXiaoyan MaoZheng YanBin LiJian MuZhou ZhouWenjing WangLin ZhaoJie DongYang ZengJing DuYanping KuangXiaoxi SunLin HeQing SangLei WangPublished in: Journal of assisted reproduction and genetics (2020)
These findings confirm previous studies and expand the mutational spectrum of LHCGR, which will provide genetic diagnostic marker for patients with empty follicle syndrome.