Correction: The 2019 and 2021 International workshops on Alport syndrome.
| Title: | Correction: The 2019 and 2021 International workshops on Alport syndrome. |
|---|---|
| Authors: | Daga S; Medical Genetics, University of Siena, Siena, Italy.; Med Biotech Hub and Competence Center, Department of Medical Biotechnologies, University of Siena, Siena, Italy.; Ding J; Peking University First Hospital, Beijing, China.; Deltas C; Biobank.cy Center of Excellence in Biobanking and Biomedical Research and University of Cyprus Medical School, Nicosia, Cyprus.; Savige J; Department of Medicine, Melbourne and Northern Health, The University of Melbourne, Parkville, VIC, 3050, Australia.; Lipska-Ziętkiewicz BS; Rare Diseases Centre, Clinical Genetics Unit, Department of Biology and Medical Genetics, Medical University of Gdańsk, Gdansk, Poland.; Hoefele J; Institute of Human Genetics, Klinikum rechts der Isar, Technical University of Munich, School of Medicine, Munich, Germany.; Flinter F; Department of Clinical Genetics, Guys' and St Thomas' NHS Foundation Trust, London, UK.; Gale DP; Department of Renal Medicine, University College London, London, UK.; Rare Renal Disease Registry, UK Renal Registry, Bristol, UK.; Aksenova M; Y. Veltischev Research and Clinical Institute for Pediatrics at the Pirogov Russian National Research Medical University, Taldomskaya Street, 2, Moscow, 125412, Russia.; Kai H; Department of Molecular Medicine, Kumamoto University, Kumamoto, Japan.; Perin L; GOFARR Laboratory for Organ Regenerative Research and Cell Therapeutics in Urology, Saban Research Institute, Division of Urology, Children's Hospital Los Angeles, Los Angeles, CA, USA.; Department of Urology, Keck School of Medicine, University of Southern California, Los Angeles, CA, USA.; Barua M; Toronto General Hospital, Toronto General Research Institute, University of Toronto, Toronto, ON, Canada.; Torra R; Inherited Kidney Diseases, Nephrology Department, Fundació Puigvert, IIB-Sant Pau, Medicine Department, Universitat Autónoma de Barcelona, Barcelona, Spain.; Miner JH; Division of Nephrology, Washington University School of Medicine, St. Louis, MO, 63110, USA.; Massella L; Division of Nephrology, Department of Pediatric Subspecialties, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.; Ljubanović DG; University of Zagreb School of Medicine, Department of Pathology and Department of Nephropathology and Electron Microscopy Dubrava University Hospital, Zagreb, Croatia.; Lennon R; Wellcome Centre for Cell-Matrix Research, Division of Cell-Matrix Biology and Regenerative Medicine, School of Biological Sciences, Faculty of Biology Medicine and Health, The University of Manchester, Manchester Academic Health Science Centre, Manchester, UK.; Weinstock AB; Alport Syndrome Foundation, Phoenix, AZ, USA.; Knebelmann B; Nephrology Department, Reference Center for Inherited Kidney Diseases (MARHEA), APHP, Necker Hospital, Paris University, Paris, France.; Cerkauskaite A; Faculty of Medicine, Vilnius University, Vilnius, Lithuania.; Vilnius University Hospital Santaros Klinikos, Vilnius, Lithuania.; Gear S; Alport UK, Tetbury, UK.; Gross O; Department of Nephrology and Rheumatology, University Medicine Goettingen, Gottingen, Germany.; Turner AN; Centre for Inflammation, University of Edinburgh, Edinburgh, UK.; Baldassarri M; Medical Genetics, University of Siena, Siena, Italy.; Med Biotech Hub and Competence Center, Department of Medical Biotechnologies, University of Siena, Siena, Italy.; Genetica Medica, Azienda Ospedaliero-Universitaria Senese, Siena, Italy.; Pinto AM; Genetica Medica, Azienda Ospedaliero-Universitaria Senese, Siena, Italy.; Renieri A; Medical Genetics, University of Siena, Siena, Italy. alessandra.renieri@unisi.it.; Med Biotech Hub and Competence Center, Department of Medical Biotechnologies, University of Siena, Siena, Italy. alessandra.renieri@unisi.it.; Genetica Medica, Azienda Ospedaliero-Universitaria Senese, Siena, Italy. alessandra.renieri@unisi.it. |
| Source: | European journal of human genetics : EJHG [Eur J Hum Genet] 2024 Jan; Vol. 32 (1), pp. 130. |
| Publication Type: | Published Erratum |
| Language: | English |
| Journal Info: | Publisher: Nature Publishing Group Country of Publication: England NLM ID: 9302235 Publication Model: Print Cited Medium: Internet ISSN: 1476-5438 (Electronic) Linking ISSN: 10184813 NLM ISO Abbreviation: Eur J Hum Genet Subsets: MEDLINE; PubMed not MEDLINE |
| Imprint Name(s): | Publication: : London : Nature Publishing Group; Original Publication: Basel ; New York : Karger, [1992- |
| Comments: | Erratum for: Eur J Hum Genet. 2022 May;30(5):507-516. doi: 10.1038/s41431-022-01075-0.. (PMID: 35260866) |
| Entry Date(s): | Date Created: 20230123 Latest Revision: 20240110 |
| Update Code: | 20260130 |
| PubMed Central ID: | PMC10772067 |
| DOI: | 10.1038/s41431-023-01286-z |
| PMID: | 36690832 |
| Database: | MEDLINE |
Published Erratum