Associated Papers
Genetic landscape of human oocyte/embryo defects.
Chen B et al.
Cell Genomics, 2026
41005306 (PubMed )
Supplement: mmc3.xlsx › Table_S2
Novel Genetic Variants in PATL2 Corresponding to Different Clinical Phenotypes of Female Infertility.
Yang X et al.
International Journal of Medical Sciences, 2025
Identification of a PATL2 missense variant (c.877G>T) disrupting canonical splicing and contributing to female infertility.
Li H et al.
Frontiers in Genetics, 2025
Genetic variants underlying developmental arrests in human preimplantation embryos.
Ozturk S
Molecular Human Reproduction, 2023
High carrier frequency of pathogenic PATL2 gene mutations predicted in population: a bioinformatics-based approach.
Zhou H et al.
Frontiers in Genetics, 2023
Identification and characterization of a novel homozygous splice site variant of PATL2 causing female infertility due to oocyte germinal vesicle arrest.
Sun L et al.
Frontiers in Genetics, 2022
Meiosis interrupted: the genetics of female infertility via meiotic failure.
Biswas L et al.
Reproduction (cambridge, England), 2021
Novel mutations in PATL2: expanding the mutational spectrum and corresponding phenotypic variability associated with female infertility.
Wu L et al.
Journal of Human Genetics, 2019
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