Novel MEI1 mutations cause chromosomal and DNA methylation abnormalities leading to embryonic arrest and implantation failure
Author:
Funder
Basic Scientific Research Funds of Department of Education of Zhejiang Province
Publisher
Springer Science and Business Media LLC
Link
https://link.springer.com/content/pdf/10.1007/s00438-024-02113-w.pdf
Reference27 articles.
1. Ben Khelifa M, Ghieh F, Boudjenah R, Hue C, Fauvert D et al (2018) A MEI1 homozygous missense mutation associated with meiotic arrest in a consanguineous family. Hum Reprod 33(6):1034–1037
2. Cahoon CK, Libuda DE (2019) Leagues of their own: sexually dimorphic features of meiotic prophase I. Chromosoma 128(3):199–214
3. Carofiglio F, Inagaki A, de Vries S, Wassenaar E, Schoenmakers S et al (2013) SPO11-independent DNA repair foci and their role in meiotic silencing. PLoS Genet 9(6):e1003538
4. Chen J, Li FH, Xing JH, Zhang XB, Du ZL et al (2022) Novel MEI1 compound heterozygous mutation in a sporadic family associated with spermatogenetic failure. Asian J Androl 25(4):544–546
5. Coticchio G, Barrie A, Lagalla C, Borini A, Fishel S et al (2021) Plasticity of the human preimplantation embryo: developmental dogmas, variations on themes and self-correction. Hum Reprod Update 27(5):848–865
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