Associated Papers
A recurrent ZP1 variant is responsible for oocyte maturation defect with degenerated oocytes in infertile females.
Loeuillet C et al.
Clinical Genetics, 2022
A novel homozygous nonsense mutation in zona pellucida 1 (ZP1) causes human female empty follicle syndrome.
Wang J et al.
Journal of Assisted Reproduction and Genetics, 2021
Novel ZP1 pathogenic variants identified in an infertile patient and a successful live birth following ICSI treatment.
Chu K et al.
Clinical Genetics, 2020
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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