Associated Papers
Novel homozygous mutation in IQCN gene causes male infertility and fertilization failure in a consanguineous mating family.
Shi L et al.
International Journal of Gynaecology and Obstetrics: the Official Organ of the International Federation of Gynaecology and Obstetrics, 2025
Biallelic variants in IQCN cause sperm flagellar assembly defects and male infertility.
Li Q et al.
Human Reproduction (oxford, England), 2023
Biallelic mutations in IQCN, encoding a novel acroplaxome protein, lead to fertilization failure and male infertility with defects in the acrosome and shaping of the spermatid head in humans and mice.
Sha Y et al.
Life Medicine, 2023
IQCN disruption causes fertilization failure and male infertility due to manchette assembly defect.
Dai J et al.
Embo Molecular Medicine, 2022
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