Associated Papers
Advances in monogenic female infertility.
Gu H et al.
Journal of Genetics and Genomics = Yi Chuan Xue Bao, 2025
Novel MEIOB pathogenic variants including a homozygous non-canonical splicing variant, cause meiotic arrest and human non-obstructive azoospermia.
Zhu X et al.
Clinical Genetics, 2024
Novel MEIOB variants cause primary ovarian insufficiency and non-obstructive azoospermia.
Wang Y et al.
Frontiers in Genetics, 2022
A truncating MEIOB mutation responsible for familial primary ovarian insufficiency abolishes its interaction with its partner SPATA22 and their recruitment to DNA double-strand breaks.
Caburet S et al.
Ebiomedicine, 2019
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