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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dc.contributor.authorKarakaya, Cengiz
dc.contributor.authorCil, Aylin Pelin
dc.contributor.authorBilguvar, Kaya
dc.contributor.authorCakir, Tunahan
dc.contributor.authorKaralok, Mete Hakan
dc.contributor.authorKarabacak, Recep Onur
dc.contributor.authorCaglayan, Ahmet Okay
dc.date.accessioned2025-10-16T15:17:48Z
dc.date.issued2022
dc.identifier.doi10.1111/jog.15187
dc.identifier.otherWOS:000753285600001
dc.identifier.urihttps://openaccess.acibadem.edu.tr/handle/11443/7012
dc.publisherWILEY
dc.sourceJOURNAL OF OBSTETRICS AND GYNAECOLOGY RESEARCH
dc.subjectextracellular matrix
dc.subjectgenetics
dc.subjectPCOS
dc.subjectwhole\\-exome sequencing
dc.titleFurther delineation of familial polycystic ovary syndrome (PCOS) via whole-exome sequencing: PCOS-related rare FBN3 and FN1 gene variants are identified
dc.typeArticle

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