Case Report: A Novel Heterozygous ZP3 Deletion Associated With Empty Follicle Syndrome and Abnormal Follicular Development

Background: Empty follicle syndrome (EFS) is defined as the complete failure to retrieve oocytes after ovarian stimulation. Although several mutations in ZP1, ZP2, ZP3, and LHCGR have been identified as genetic causes of EFS, its pathogenesis is still not well-understood. Methods: Whole-exome sequen...

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Detalles Bibliográficos
Autores principales: Chen, Yongzhe, Wang, Zesong, Wu, Yueren, He, Wenbin, Du, Juan, Cai, Sufen, Gong, Fei, Lu, Guangxiu, Lin, Ge, Dai, Can
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8170154/
https://www.ncbi.nlm.nih.gov/pubmed/34093671
http://dx.doi.org/10.3389/fgene.2021.690070

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8170154/
https://www.ncbi.nlm.nih.gov/pubmed/34093671
http://dx.doi.org/10.3389/fgene.2021.690070

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