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作者机构:Suna and İnan Kıraç Foundation Neurodegeneration Research Laboratory (NDAL) Research Center for Translational Medicine (KUTTAM) Koç University School of Medicine Istanbul Turkey Suna and İnan Kıraç Foundation Neurodegeneration Research Laboratory (NDAL) Department of Molecular Biology and Genetics Boğaziçi University Istanbul Turkey Genomize Inc. Boğaziçi University Technology Development Region Istanbul Turkey Department of Computer Engineering Bilkent University Ankara Turkey Department of Anesthesiology and Reanimation American Hospital Istanbul Turkey Department of Neurology Istanbul Medical School Istanbul University Istanbul Turkey Department of Neurology Faculty of Medicine Bezmialem Vakıf University Istanbul Turkey Department of Neurology Marmara University School of Medicine Istanbul Turkey Department of Neurology Namık Kemal University School of Medicine Tekirdağ Turkey Department of Neurology Medipol University School of Medicine Istanbul Turkey Department of Neurology Karadeniz Technical University School of Medicine Trabzon Turkey Department of Neurology Faculty of Medicine Sakarya University Sakarya Turkey Department of Neurology Bakırköy Research and Training Hospital for Neurologic and Psychiatric Diseases Istanbul Turkey Department of Neurology Cerrahpaşa Medical School Istanbul University-Cerrahpaşa Istanbul Turkey Department of Neurology Çukurova University Medical School Adana Turkey Department of Neurology Hacettepe University Medical School Ankara Turkey Department of Computer Science and Engineering Sabancı University Istanbul Turkey Department of Computational Biology Carnegie Mellon University Pittsburgh Pennsylvania
出 版 物:《Human Mutation》 (人类突变)
年 卷 期:2020年第41卷第8期
页 面:ii-ii页
学科分类:0710[理学-生物学] 071010[理学-生物化学与分子生物学] 07[理学]
摘 要:The cover image is based on the Research Article Genotype‐phenotype associations in a large PRPH2‐related retinopathy cohort by Melissa J. Reeves et al., https://***/10.1002/humu.24065.