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

Autor: Kina BG; Department of Genetics, Aziz Sancar Institute of Experimental Medicine, Istanbul University, Istanbul, Turkey.; Graduate School of Health Sciences, Istanbul University, Istanbul, Turkey., Topbas Selcuki NF; Department of Obstetrics and Gynecology, Istanbul Sisli Hamidiye Etfal Training and Research Hospital, University of Health Sciences Turkiye, Istanbul, Turkey., Bahat PY; Department of Obstetrics and Gynecology, Istanbul Kanuni Sultan Suleyman Training and Research Hospital, University of Health Sciences Turkiye, Istanbul, Turkey., Usta T; Department of Obstetrics and Gynecology, Acibadem Altunizade Hospital, Mehmet Ali Aydinlar University, Istanbul, Turkey., Aydin S; Department of Genetics, Aziz Sancar Institute of Experimental Medicine, Istanbul University, Istanbul, Turkey.; Graduate School of Health Sciences, Istanbul University, Istanbul, Turkey., Rahmioglu N; Oxford Endometriosis Care Centre, Nuffield Department of Women's and Reproductive Health, University of Oxford, Women's Centre, John Radcliffe Hospital, Oxford, UK.; Wellcome Centre for Human Genetics, University of Oxford, Oxford, UK., Tuncer FN; Department of Genetics, Aziz Sancar Institute of Experimental Medicine, Istanbul University, Istanbul, Turkey., Oral E; Department of Obstetrics and Gynecology, Bezmialem Vakif University, Istanbul, Turkey.

Publikováno v: Molecular genetics & genomic medicine [Mol Genet Genomic Med] 2024 Jan; Vol. 12 (1), pp. e2312. Date of Electronic Publication: 2023 Nov 27.