Heterozygous FMN2 missense variant found in a family case of premature ovarian insufficiency.
Jie LiTianliu PengLe WangPanpan LongRuping QuanHangjing TanMinghua ZengXue WuJunting YangHong-Mei XiaoXiaobo ShiPublished in: Journal of ovarian research (2022)
This finding indicates a novel gene possibly related to POI and sheds lights on the study of FMN2.