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MON-207 Identification of Monogenic Causes of Polycystic Ovary Syndrome by High Throughput Sequencing
BACKGROUND: Polycystic ovary syndrome (PCOS) is a common complex endocrine disorder, whose etiology remains to be elucidated. PCOS has a strong heritable component. Genome-wide association studies have identified several risk loci for PCOS; however, the identified candidate genes could explain less...
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| Publicado no: | J Endocr Soc |
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| Main Authors: | , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Endocrine Society
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6550938/ https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/js.2019-MON-207 |
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