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The contribution of rare genetic variants to the pathogenesis of polycystic ovary syndrome
Polycystic ovary syndrome (PCOS) is a highly heritable disorder, but only a small proportion of the heritability can be accounted for by common genetic risk variants identified to date. It is possible that variants with lower allele frequencies that cannot be detected using genome-wide association s...
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| Publicado no: | Curr Opin Endocr Metab Res |
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| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7241430/ https://ncbi.nlm.nih.gov/pubmed/32440573 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.coemr.2020.02.011 |
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