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The 2019 and 2021 International Workshops on Alport Syndrome

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第一作者: Sergio,Daga
作者单位: Medical Genetics,University of Siena [1] Peking University First Hospital [2] Biobank.cy Center of Excellence in Biobanking and Biomedical Research and University of Cyprus [3] Department of Medicine, Melbourne and Northern Health,The University of Melbourne [4] Rare Diseases Centre, Clinical Genetics Unit, Department of Biology and Medical Genetics,Medical [5] Institute of Human Genetics, Klinikum rechts der Isar,Technical University of Munich, School of [6] Department of Clinical Genetics,Guys’ and St Thomas’ NHS Foundation Trust [7] Department of Renal Medicine,University College London [8] Y. Veltischev Research and Clinical Institute for Pediatrics at the Pirogov Russian National [9] Department of Molecular Medicine,Kumamoto University [10] GOFARR Laboratory for Organ Regenerative Research and Cell Therapeutics in Urology, Saban Research [11] Toronto General Hospital, Toronto General Research Institute,University of Toronto [12] Inherited Kidney Diseases, Nephrology Department, Fundació Puigvert, IIB-Sant Pau, Medicine [13] Division of Nephrology,Washington University School of Medicine [14] Division of Nephrology, Department of Pediatric Subspecialties,Bambino Gesù Children’s Hospital [15] University of Zagreb School of Medicine, Department of Pathology and Department of Nephropathology [16] Wellcome Centre for Cell-Matrix Research, Division of Cell-Matrix Biology and Regenerative Medicine [17] Alport Syndrome Foundation [18] Nephrology Department, Reference Center for Inherited Kidney Diseases (MARHEA), APHP, Necker [19] Faculty of Medicine,Vilnius University [20] Alport UK [21] Department of Nephrology and Rheumatology,University Medicine Goettingen [22] Centre for Inflammation,University of Edinburgh [23] Genetica Medica,Azienda Ospedaliero-Universitaria Senese [24]
发布时间 2022-07-29
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