Correction: Consensus statement on standards and guidelines for the molecular diagnostics of Alport syndrome: refining the ACMG criteria.
| Title: | Correction: Consensus statement on standards and guidelines for the molecular diagnostics of Alport syndrome: refining the ACMG criteria. |
|---|---|
| Authors: | Savige J; Department of Medicine (MH and NH), The University of Melbourne, Parkville, VIC, Australia. jasavige@unimelb.edu.au.; Storey H; Molecular Genetics, Viapath Laboratories, Guy's Hospital, London, UK.; Watson E; Elizabeth Watson, South West Genomic Laboratory Hub, North Bristol Trust, Bristol, UK.; Hertz JM; Jens Michael Hertz, Department of Clinical Genetics, Odense University Hospital, Odense, Denmark.; Deltas C; Center of Excellence in Biobanking and Biomedical Research and Molecule Medicine Center, University of Cyprus, Nicosia, Cyprus.; Renieri A; Medical Genetics, University of Siena, Siena, Italy.; Mari F; Institute de Pathologie et de Genetique ASBL, Departement de Biologie Moleculaire, Gosselies, Belgium.; Hilbert P; Institute de Pathologie et de Genetique ASBL, Departement de Biologie Moleculaire, Gosselies, Belgium.; Plevova P; Department of Medical Genetics, and Department of Biomedical Sciences, University Hospital of Ostrava, Ostrava, Czech Republic.; Byers P; Departments of Pathology and Medicine (Medical Genetics), University of Washington, Seattle, WA, USA.; Cerkauskaite A; Institute of Biomedical Sciences, Faculty of Medicine, Vilnius University, Vilnius, Lithuania.; Gregory M; Division of Nephrology, Department of Medicine, University of Utah Health, Salt Lake City, UT, USA.; Cerkauskiene R; Clinic of Pediatrics, Institute of Clinical Medicine, Faculty of Medicine, Vilnius University, Vilnius, Lithuania.; Ljubanovic DG; Department of Pathology, University of Zagreb, School of Medicine, Dubrava University Hospital, Zagreb, Croatia.; Becherucci F; Nephrology Unit and Meyer Children's University Hospital, Firenze, Italy.; Errichiello C; Nephrology Unit and Meyer Children's University Hospital, Firenze, Italy.; Massella L; Division of Nephrology and Dialysis, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.; Aiello V; Department of Experimental Diagnostic and Specialty Medicine (DIMES), Nephrology, Dialysis and Renal Transplant Unit, S. Orsola Hospital, University of Bologna, Bologna, Italy.; 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, UK.; Hopkinson L; 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, UK.; Koziell A; School of Immunology and Microbial Sciences, Faculty of Life Sciences, King's College London, London, UK.; Lungu A; Fundeni Clinical Institute, Pediatric Nephrology Department, Bucharest, Romania.; Rothe HM; Centre for Nephrology and Metabolic Disorders, Weisswasser, Germany.; Hoefele J; Institute of Human Genetics, Technical University of Munich, München, Germany.; Zacchia M; Nephrology Unit, University of Campania, Naples, Italy.; Martic TN; Department of Biology, School of Medicine University of Zagreb, Zagreb, Croatia.; Gupta A; Birmingham Children's Hospital, Birmingham, UK.; van Eerde A; Departments of Genetics and Center for Molecular Medicine, University Medical Center, Utrecht University, Utrecht, The Netherlands.; Gear S; Alport UK, Gloucester, UK.; Landini S; Medical Genetics Unit, Department of Clinical and Experimental Biomedical Sciences 'Mario Serio', University of Florence, Florence, Italy.; Palazzo V; Medical Genetics Unit, Meyer Children's University Hospital, Florence, Italy.; Al-Rabadi L; Health Sciences Centre, University of UTAH, Salt Lake City, UT, USA.; Claes K; Department of Nephrology and Renal Transplantation, University Hospitals Leuven, Leuven, Belgium.; Corveleyn A; Center for Human Genetics, University Hospitals and KU Leuven, Leuven, Belgium.; Van Hoof E; Center for Human Genetics, University Hospitals and KU Leuven, Leuven, Belgium.; van Geel M; Department of Clinical Genetics, Maastricht University Medical Center, Maastricht, The Netherlands.; Williams M; Bristol Genetics Laboratory Pathology Sciences, Southmead Hospital, Bristol, UK.; Ashton E; North East Thames Regional Genetics Laboratory, Great Ormond Street Hospital, London, UK.; Belge H; Department of Physiology, Radboud Institute for Molecular Life Sciences, Radboud University Medical Center, Nijmegen, The Netherlands.; Ars E; Inherited Kidney Disorders, Fundacio Puigvert, Universitat Autonoma de Barcelona, Barcelona, Spain.; Bierzynska A; Bristol Renal Unit, Bristol Medical School, University of Bristol, Bristol, UK.; Gangemi C; Division of Nephrology and Dialysis, University Hospital of Verona, Verona, Italy.; Lipska-Ziętkiewicz BS; Centre for Rare Diseases, and Clinical Genetics Unit, Medical University of Gdansk, Gdansk, Poland. |
| Source: | European journal of human genetics : EJHG [Eur J Hum Genet] 2024 Jan; Vol. 32 (1), pp. 132. |
| 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. 2021 Aug;29(8):1186-1197. doi: 10.1038/s41431-021-00858-1.. (PMID: 33854215) |
| Entry Date(s): | Date Created: 20230131 Latest Revision: 20240110 |
| Update Code: | 20260130 |
| PubMed Central ID: | PMC10772080 |
| DOI: | 10.1038/s41431-023-01288-x |
| PMID: | 36721056 |
| Database: | MEDLINE |
Published Erratum