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...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:J Endocr Soc
Hauptverfasser: Crespo, Raiane, Rocha, Thais, Maciel, Gustavo, Hayashida, Sylvia, Baracat, Edmund, Lerario, Antonio, Nishi, Mirian, Latronico, Ana Claudia, Mendonca, Berenice, Gomes, Larissa
Format: Artigo
Sprache:Inglês
Veröffentlicht: Endocrine Society 2019
Schlagworte:
Reproductive Endocrinology
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC6550938/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/js.2019-MON-207
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!

Ähnliche Einträge