A novel mutation in ZP3 causes empty follicle syndrome and abnormal zona pellucida formation

PURPOSE: To identify disease-causing genes involved in female infertility. METHODS: Whole-exome sequencing and Sanger DNA sequencing were used to identify the mutations in disease-causing genes. We performed subcellular protein localization, western immunoblotting analysis, and co-immunoprecipitatio...

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Detalhes bibliográficos
Publicado no:J Assist Reprod Genet
Main Authors: Zhang, Dazhi, Zhu, Lixia, Liu, Zhenxing, Ren, Xinling, Yang, Xue, Li, Dan, Luo, Yalin, Peng, Xuejie, Zhou, Xiaopei, Jia, Weimin, Hou, Meiqi, Li, Zhou, Jin, Lei, Zhang, Xianqin
Formato: Artigo
Idioma:Inglês
Publicado em: Springer US 2020
Assuntos:
Genetics
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7822995/
https://ncbi.nlm.nih.gov/pubmed/33140178
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s10815-020-01995-0
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