High-throughput Sequencing to Identify Monogenic Etiologies in a Preselected Polycystic Ovary Syndrome Cohort

CONTEXT: Polycystic ovary syndrome (PCOS) etiology remains to be elucidated, but familial clustering and twin studies have shown a strong heritable component. OBJECTIVE: The purpose of this study was to identify rare genetic variants that are associated with the etiology of PCOS in a preselected coh...

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Detalles Bibliográficos
Autores principales: Crespo, Raiane P, Rocha, Thais P, Montenegro, Luciana R, Nishi, Mirian Y, Jorge, Alexander A L, Maciel, Gustavo A R, Baracat, Edmund, Latronico, Ana Claudia, Mendonca, Berenice B, Gomes, Larissa G
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Clinical Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9309801/
https://www.ncbi.nlm.nih.gov/pubmed/35898701
http://dx.doi.org/10.1210/jendso/bvac106

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9309801/
https://www.ncbi.nlm.nih.gov/pubmed/35898701
http://dx.doi.org/10.1210/jendso/bvac106

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