Clinical phenotype and genetic analysis of patients with severe oligoasthenospermia carrying heterozygous SOHLH1 c.346-1G>A mutation - Wen, Xiaojun; Li, Zhiming; Cheng, Lizi; Wei, Jianhong; Yu, Wenjuan; Lin, Xiufeng; Fang, Xiaowu (Frontiers in Genetics, 2025)