Associated Papers
Genetic and epigenetic insights into non-obstructive azoospermia: mechanisms, biomarkers, and clinical perspectives.
Wang X et al.
Reproductive Biology and Endocrinology : Rb&e, 2025
Bi-allelic variants in SHOC1 cause non-obstructive azoospermia with meiosis arrest in humans and mice.
Wang W et al.
Molecular Human Reproduction, 2022
Bi-allelic SHOC1 loss-of-function mutations cause meiotic arrest and non-obstructive azoospermia.
Yao C et al.
Journal of Medical Genetics, 2021
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