Associated Papers
ZP1-Y262C mutation causes abnormal zona pellucida formation and female infertility in humans.
Cao G et al.
Frontiers in Genetics, 2024
Homozygous Splice Site Mutation in ZP1 Causes Familial Oocyte Maturation Defect.
Okutman Ö et al.
Genes, 2020
ZP1 mutations are associated with empty follicle syndrome: evidence for the existence of an intact oocyte and a zona pellucida in follicles up to the early antral stage. A case report.
Dai C et al.
Human Reproduction (oxford, England), 2019
Genetic variations in zona pellucida glycoproteins: Implications for fertility and ART outcomes.
Rajput N et al.
Mutation Research. Reviews in Mutation Research, 0
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