Whole exome sequencing reveals novel candidate variants for endometriosis utilizing multiple affected members in a single family

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dc.contributor.authorKina, Busra Gizem
dc.contributor.authorSelcuki, Nura Fitnat Topbas
dc.contributor.authorBahat, Pinar Yalcin
dc.contributor.authorUsta, Taner
dc.contributor.authorAydin, Sevcan
dc.contributor.authorRahmioglu, Nilufer
dc.contributor.authorTuncer, Feyza Nur
dc.contributor.authorOral, Engin
dc.date.accessioned2025-10-16T15:14:11Z
dc.date.issued2024
dc.identifier.doi10.1002/mgg3.2312
dc.identifier.otherWOS:001110048800001
dc.identifier.urihttps://openaccess.acibadem.edu.tr/handle/11443/6088
dc.publisherWILEY
dc.sourceMOLECULAR GENETICS \& GENOMIC MEDICINE
dc.subjectendometrial serous adenocarcinoma
dc.subjectendometriosis
dc.subjectfamily
dc.subjectnovel genetic variants
dc.subjectwhole exome sequencing
dc.titleWhole exome sequencing reveals novel candidate variants for endometriosis utilizing multiple affected members in a single family
dc.typeArticle

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