NOBOX突变在卵巢功能不全中的研究进展

Asma Sassi, J. Désir, A. Gheldof, S. Dooren, Xavier Peyrassol, M. Abramowicz, A. Delbaere
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摘要

Asma Sassi1, Julie dsamsi2, Alexander Gheldof3, Sonia Van Dooren4, Xavier Peyrassol5, Marc Abramowicz5, Anne Delbaere1* 1比利时布鲁塞尔布鲁塞尔自由大学Erasme医院妇产科生育诊所2比利时Gosselies病理与遗传研究所(IPG) 3医学遗传学、生殖与遗传学和再生医学研究集群中心,生殖与遗传学研究小组,布鲁塞尔自由大学,布鲁塞尔布鲁塞尔,比利时4布鲁塞尔大学间基因组学高通量中心(Bright core),比利时布鲁塞尔5布鲁塞尔自由大学伊拉斯姆医院遗传学系,比利时布鲁塞尔6日内瓦大学医学院遗传医学与发展学系,日内瓦1211,瑞士*信件请寄给Anne Delbaere, anne.delbaere@erasme.ulb.ac.be
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Commentary on NOBOX Mutations in Premature Ovarian Insufficiency
Asma Sassi1, Julie Désir2, Alexander Gheldof3, Sonia Van Dooren4, Xavier Peyrassol5, Marc Abramowicz5, Anne Delbaere1* 1Fertility Clinic, Department of Obstetrics and Gynecology, Erasme Hospital, Université Libre de Bruxelles, Brussels, Belgium 2Institut de Pathologie et de Génétique (IPG), Gosselies, Belgium 3Centre for Medical Genetics, Reproduction and Genetics and Regenerative Medicine research cluster, Reproduction and Genetics research group, Vrije Universiteit Brussel-UZ Brussel, Brussels, Belgium 4Brussels Interuniversity Genomics High Throughput core (Bright Core), Brussels, Belgium 5Department of Genetics, Erasme Hospital, Université Libre de Bruxelles, Brussels, Belgium 6Department of Genetic Medicine and Development, Faculty of Medicine, University of Geneva, 1211 Geneva, Switzerland *Correspondence should be addressed to Anne Delbaere, anne.delbaere@erasme.ulb.ac.be
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