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
Genetic variants underlying spermatogenic arrests in men with non-obstructive azoospermia.
Ozturk S
Cell Cycle (georgetown, Tex.), 2023
A homozygous loss-of-function mutation in FBXO43 causes human non-obstructive azoospermia.
Wu H et al.
Clinical Genetics, 2022
FBXO43 variants in patients with female infertility characterized by early embryonic arrest.
Wang W et al.
Human Reproduction (oxford, England), 2021
A novel homozygous FBXO43 mutation associated with male infertility and teratozoospermia in a consanguineous Chinese family.
Ma Y et al.
Fertility and Sterility, 2019
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