Exome‐based genome‐wide screening of rare variants associated with the risk of polycystic ovary syndrome

PURPOSE: Genetic factors associated with the risk of polycystic ovary syndrome (PCOS) remain largely unknown. Here, we conducted an optimal sequence kernel association test (SKAT‐O), an exome‐based rare variant association study, to clarify whether rare variants in specific genes contribute to the d...

Descripción completa

Detalles Bibliográficos
Autores principales: Tamaoka, Satoshi, Saito, Kazuki, Yoshida, Tomoko, Nakabayashi, Kazuhiko, Tatsumi, Kenichi, Kawamura, Toshihiro, Matsuzaki, Toshiya, Matsubara, Keiko, Ogata‐Kawata, Hiroko, Hata, Kenichiro, Kato‐Fukui, Yuko, Fukami, Maki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9947624/
https://www.ncbi.nlm.nih.gov/pubmed/36845002
http://dx.doi.org/10.1002/rmb2.12504

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9947624/
https://www.ncbi.nlm.nih.gov/pubmed/36845002
http://dx.doi.org/10.1002/rmb2.12504

Ejemplares similares