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Familial bilateral cryptorchidism is caused by recessive variants in RXFP2
BACKGROUND: Cryptorchidism or failure of testicular descent is the most common genitourinary birth defect in males. While both the insulin-like peptide 3 (INSL3) and its receptor, relaxin family peptide receptor 2 (RXFP2), have been demonstrated to control testicular descent in mice, their link to h...
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| Опубликовано в: : | J Med Genet |
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| Главные авторы: | , , , , , , , |
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
BMJ Publishing Group
2019
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| Предметы: | |
| Online-ссылка: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6860408/ https://ncbi.nlm.nih.gov/pubmed/31167797 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmedgenet-2019-106203 |
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