טוען...
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...
שמור ב:
| הוצא לאור ב: | J Assist Reprod Genet |
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| Main Authors: | , , , , , , , , , , , , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
Springer US
2020
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| נושאים: | |
| גישה מקוונת: | 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 |
| תגים: |
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