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Investigating the role of common and rare variants in multiplex multiple sclerosis families reveals an increased burden of common risk variation.

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第一作者: Elif,Everest
第一单位: Department of Molecular Biology and Genetics, Faculty of Science and Letters, Istanbul Technical University, Maslak, Istanbul, Turkey.
作者单位: Department of Molecular Biology and Genetics, Faculty of Science and Letters, Istanbul Technical University, Maslak, Istanbul, Turkey. [1] Department of Psychiatry, Virginia Institute for Psychiatric and Behavioral Genetics, Virginia Commonwealth University, Richmond, VA, USA. [2] Department of Neurology, Cerrahpasa School of Medicine, Istanbul University-Cerrahpasa, Fatih, Istanbul, Turkey. [3] Department of Biostatistics and Bioinformatics, Institute of Health Sciences, Acibadem University, Atasehir, Istanbul, Turkey. [4] Department of Neurology, Tayfur Ata Sokmen School of Medicine, Mustafa Kemal University, Alahan-Antakya, Hatay, Turkey. [5] Department of Biostatistics and Medical Informatics, Faculty of Medicine, Acibadem University, Atasehir, Istanbul, Turkey. [6] Translational Neuroradiology Section, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD, USA. [7] Department of Psychiatry and Human and Molecular Genetics, Virginia Institute for Psychiatric and Behavioral Genetics, Virginia Commonwealth University, Richmond, VA, USA. [8] Department of Molecular Biology and Genetics, Faculty of Engineering and Natural Sciences, Acibadem University, Atasehir, Istanbul, Turkey. eda.turanli@acibadem.edu.tr.;Molecular and Translational Biomedicine Program, Graduate School of Natural and Applied Sciences, Acibadem University, Atasehir, Istanbul, Turkey. eda.turanli@acibadem.edu.tr. [9]
DOI 10.1038/s41598-022-21484-x
PMID 36216875
发布时间 2024-11-16
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