Novel mutations of PMFBP1 in a man with acephalic spermatozoa defects
Abstract Background Acephalic spermatozoa (AS) is a serious but rare reproductive genetic disorder that causes infertility in men. To date, only a few genes associated with AS defects have been identified, including the polyamine modulated factor 1 binding protein 1 (PMFBP1) gene. Consistent with th...
Kaydedildi:
| Asıl Yazarlar: | , , , , |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Wiley
2022-09-01
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| Seri Bilgileri: | Molecular Genetics & Genomic Medicine |
| Konular: | |
| Online Erişim: | https://doi.org/10.1002/mgg3.2020 |
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