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Variants in RABL2A causing male infertility and ciliopathy
Approximately 7% of men worldwide suffer from infertility, with sperm abnormalities being the most common defect. Though genetic causes are thought to underlie a substantial fraction of idiopathic cases, the actual molecular bases are usually undetermined. Because the consequences of most genetic va...
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| Veröffentlicht in: | Hum Mol Genet |
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| Hauptverfasser: | , , , , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
Oxford University Press
2020
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7749704/ https://ncbi.nlm.nih.gov/pubmed/33075816 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddaa230 |
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