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Heterozygous mutations in ZP1 and ZP3 cause formation disorder of ZP and female infertility in human
The human zona pellucida (ZP) is a highly organized glycoprotein matrix that encircles oocytes and plays an essential role in successful reproduction. Previous studies have reported that mutations in human ZP1, ZP2 and ZP3 influence their functions and result in a lack of ZP or in an abnormal oocyte...
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| Publicado no: | J Cell Mol Med |
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| Main Authors: | , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
John Wiley and Sons Inc.
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7412702/ https://ncbi.nlm.nih.gov/pubmed/32573113 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/jcmm.15482 |
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