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

Autor: Cengiz Karakaya, Aylin Pelin Çil, Kaya Bilguvar, Tunahan Çakir, Mete Hakan Karalok, Recep Onur Karabacak, Ahmet Okay Caglayan
Rok vydání: 2022
Předmět:
Zdroj: Journal of Obstetrics and Gynaecology Research. 48:1202-1211
ISSN: 1447-0756
1341-8076
DOI: 10.1111/jog.15187
Databáze: OpenAIRE
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