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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Publicat a:J Endocr Soc
Autors principals: Crespo, Raiane, Rocha, Thais, Maciel, Gustavo, Hayashida, Sylvia, Baracat, Edmund, Lerario, Antonio, Nishi, Mirian, Latronico, Ana Claudia, Mendonca, Berenice, Gomes, Larissa
Format: Artigo
Idioma:Inglês
Publicat: Endocrine Society 2019
Matèries:
Reproductive Endocrinology
Accés en línia: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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