Loss-of-function variants in KCTD19 cause non-obstructive azoospermia in humans
Summary: Azoospermia is a significant cause of male infertility, with non-obstructive azoospermia (NOA) being the most severe type of spermatogenic failure. NOA is mostly caused by congenital factors, but our understanding of its genetic causes is very limited. Here, we identified a frameshift varia...
Kaydedildi:
| Asıl Yazarlar: | , , , , , , , , , , , , , , , , , , , , , , , , |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Elsevier
2023-07-01
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| Seri Bilgileri: | iScience |
| Konular: | |
| Online Erişim: | http://www.sciencedirect.com/science/article/pii/S2589004223012701 |
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