"Further delineation of familial polycystic ovary syndrome (PCOS) via whole‐exome sequencing: PCOS‐related rare FBN3 and FN1 gene variants are identified"

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To identify pathogenic rare coding Mendelian/high‐effect size variant(s) by whole‐exome sequencing in familial polycystic ovary syndrome (PCOS) patients to elucidate PCOS‐related pathways. Click to show full abstract

To identify pathogenic rare coding Mendelian/high‐effect size variant(s) by whole‐exome sequencing in familial polycystic ovary syndrome (PCOS) patients to elucidate PCOS‐related pathways.

Keywords: familial polycystic; exome sequencing; polycystic ovary; ovary syndrome; whole exome; syndrome pcos

Journal Title: Journal of Obstetrics and Gynaecology Research
Year Published: 2022

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