Correction: Consensus statement on standards and guidelines for the molecular diagnostics of Alport syndrome: refining the ACMG criteria

Savige, Judy; Storey, Helen; Watson, Elizabeth; Hertz, Jens Michael; Deltas, Constantinos; Renieri, Alessandra; Mari, Francesca; Hilbert, Pascale; Plevova, Pavlina; Byers, Peter; Cerkauskaite, Agne; Gregory, Martin; Cerkauskiene, Rimante; Ljubanovic, Danica Galesic; Becherucci, Francesca; Errichiello, Carmela; Massella, Laura; Aiello, Valeria; Lennon, Rachel; Hopkinson, Louise; Koziell, Ania; Lungu, Adrian; Rothe, Hansjorg Martin; Hoefele, Julia; Zacchia, Miriam; Martic, Tamara Nikuseva; Gupta, Asheeta; van Eerde, Albertien; Gear, Susie; Landini, Samuela; Palazzo, Viviana; al-Rabadi, Laith; Claes, Kathleen; Corveleyn, Anniek; Van Hoof, Evelien; van Geel, Micheel; Williams, Maggie; Ashton, Emma; Belge, Hendica; Ars, Elisabeth; Bierzynska, Agnieszka; Gangemi, Concetta; Lipska-Ziętkiewicz, Beata S.

doi:10.1038/s41431-023-01288-x

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Published: 31 January 2023

Correction: Consensus statement on standards and guidelines for the molecular diagnostics of Alport syndrome: refining the ACMG criteria

Judy Savige ORCID: orcid.org/0000-0002-6813-0288¹,
Helen Storey ORCID: orcid.org/0000-0002-2214-6444²,
Elizabeth Watson³,
Jens Michael Hertz⁴,
Constantinos Deltas ORCID: orcid.org/0000-0001-5549-9169⁵,
Alessandra Renieri ORCID: orcid.org/0000-0002-0846-9220⁶,
Francesca Mari⁷,
Pascale Hilbert ORCID: orcid.org/0000-0003-4540-4538⁷,
Pavlina Plevova⁸,
Peter Byers⁹,
Agne Cerkauskaite¹⁰,
Martin Gregory¹¹,
Rimante Cerkauskiene¹²,
Danica Galesic Ljubanovic¹³,
Francesca Becherucci¹⁴,
Carmela Errichiello¹⁴,
Laura Massella¹⁵,
Valeria Aiello¹⁶,
Rachel Lennon¹⁷,
Louise Hopkinson ORCID: orcid.org/0000-0003-1758-4201¹⁷,
Ania Koziell¹⁸,
Adrian Lungu¹⁹,
Hansjorg Martin Rothe ORCID: orcid.org/0000-0003-1163-6576²⁰,
Julia Hoefele ORCID: orcid.org/0000-0002-7917-7129²¹,
Miriam Zacchia²²,
Tamara Nikuseva Martic²³,
Asheeta Gupta²⁴,
Albertien van Eerde²⁵,
Susie Gear²⁶,
Samuela Landini ORCID: orcid.org/0000-0001-7423-0325²⁷,
Viviana Palazzo²⁸,
Laith al-Rabadi²⁹,
Kathleen Claes ORCID: orcid.org/0000-0001-8510-2345³⁰,
Anniek Corveleyn³¹,
Evelien Van Hoof³¹,
Micheel van Geel³²,
Maggie Williams³³,
Emma Ashton³⁴,
Hendica Belge³⁵,
Elisabeth Ars³⁶,
Agnieszka Bierzynska³⁷,
Concetta Gangemi³⁸ &
…
Beata S. Lipska-Ziętkiewicz³⁹

European Journal of Human Genetics volume 32, page 132 (2024)Cite this article

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The Original Article was published on 15 April 2021

Correction to: European Journal of Human Genetics (2021) 29:1186–1197 https://doi.org/10.1038/s41431-021-00858-1

The following Acknowledgement was missing:

This research has been supported not financially by “European Reference Network for Rare Kidney Disease, ERKNet”. This ERN is partly co-funded by the European Union within the framework of the Third Health Programme “ERN- 2016 – Framework Partnership Agreement 2017–2021”.

The original article has been corrected.

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Authors and Affiliations

Department of Medicine (MH and NH), The University of Melbourne, Parkville, VIC, Australia
Judy Savige
Molecular Genetics, Viapath Laboratories, Guy’s Hospital, London, UK
Helen Storey
Elizabeth Watson, South West Genomic Laboratory Hub, North Bristol Trust, Bristol, UK
Elizabeth Watson
Jens Michael Hertz, Department of Clinical Genetics, Odense University Hospital, Odense, Denmark
Jens Michael Hertz
Center of Excellence in Biobanking and Biomedical Research and Molecule Medicine Center, University of Cyprus, Nicosia, Cyprus
Constantinos Deltas
Medical Genetics, University of Siena, Siena, Italy
Alessandra Renieri
Institute de Pathologie et de Genetique ASBL, Departement de Biologie Moleculaire, Gosselies, Belgium
Francesca Mari & Pascale Hilbert
Department of Medical Genetics, and Department of Biomedical Sciences, University Hospital of Ostrava, Ostrava, Czech Republic
Pavlina Plevova
Departments of Pathology and Medicine (Medical Genetics), University of Washington, Seattle, WA, USA
Peter Byers
Institute of Biomedical Sciences, Faculty of Medicine, Vilnius University, Vilnius, Lithuania
Agne Cerkauskaite
Division of Nephrology, Department of Medicine, University of Utah Health, Salt Lake City, UT, USA
Martin Gregory
Clinic of Pediatrics, Institute of Clinical Medicine, Faculty of Medicine, Vilnius University, Vilnius, Lithuania
Rimante Cerkauskiene
Department of Pathology, University of Zagreb, School of Medicine, Dubrava University Hospital, Zagreb, Croatia
Danica Galesic Ljubanovic
Nephrology Unit and Meyer Children’s University Hospital, Firenze, Italy
Francesca Becherucci & Carmela Errichiello
Division of Nephrology and Dialysis, Bambino Gesù Children’s Hospital, IRCCS, Rome, Italy
Laura Massella
Department of Experimental Diagnostic and Specialty Medicine (DIMES), Nephrology, Dialysis and Renal Transplant Unit, S. Orsola Hospital, University of Bologna, Bologna, Italy
Valeria Aiello
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
Rachel Lennon & Louise Hopkinson
School of Immunology and Microbial Sciences, Faculty of Life Sciences, King’s College London, London, UK
Ania Koziell
Fundeni Clinical Institute, Pediatric Nephrology Department, Bucharest, Romania
Adrian Lungu
Centre for Nephrology and Metabolic Disorders, Weisswasser, Germany
Hansjorg Martin Rothe
Institute of Human Genetics, Technical University of Munich, München, Germany
Julia Hoefele
Nephrology Unit, University of Campania, Naples, Italy
Miriam Zacchia
Department of Biology, School of Medicine University of Zagreb, Zagreb, Croatia
Tamara Nikuseva Martic
Birmingham Children’s Hospital, Birmingham, UK
Asheeta Gupta
Departments of Genetics and Center for Molecular Medicine, University Medical Center, Utrecht University, Utrecht, The Netherlands
Albertien van Eerde
Alport UK, Gloucester, UK
Susie Gear
Medical Genetics Unit, Department of Clinical and Experimental Biomedical Sciences “Mario Serio”, University of Florence, Florence, Italy
Samuela Landini
Medical Genetics Unit, Meyer Children’s University Hospital, Florence, Italy
Viviana Palazzo
Health Sciences Centre, University of UTAH, Salt Lake City, UT, USA
Laith al-Rabadi
Department of Nephrology and Renal Transplantation, University Hospitals Leuven, Leuven, Belgium
Kathleen Claes
Center for Human Genetics, University Hospitals and KU Leuven, Leuven, Belgium
Anniek Corveleyn & Evelien Van Hoof
Department of Clinical Genetics, Maastricht University Medical Center, Maastricht, The Netherlands
Micheel van Geel
Bristol Genetics Laboratory Pathology Sciences, Southmead Hospital, Bristol, UK
Maggie Williams
North East Thames Regional Genetics Laboratory, Great Ormond Street Hospital, London, UK
Emma Ashton
Department of Physiology, Radboud Institute for Molecular Life Sciences, Radboud University Medical Center, Nijmegen, The Netherlands
Hendica Belge
Inherited Kidney Disorders, Fundacio Puigvert, Universitat Autonoma de Barcelona, Barcelona, Spain
Elisabeth Ars
Bristol Renal Unit, Bristol Medical School, University of Bristol, Bristol, UK
Agnieszka Bierzynska
Division of Nephrology and Dialysis, University Hospital of Verona, Verona, Italy
Concetta Gangemi
Centre for Rare Diseases, and Clinical Genetics Unit, Medical University of Gdansk, Gdansk, Poland
Beata S. Lipska-Ziętkiewicz

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Judy Savige
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Helen Storey
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Elizabeth Watson
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Jens Michael Hertz
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Constantinos Deltas
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Correspondence to Judy Savige.

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The original article can be found online at https://doi.org/10.1038/s41431-021-00858-1.

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Savige, J., Storey, H., Watson, E. et al. Correction: Consensus statement on standards and guidelines for the molecular diagnostics of Alport syndrome: refining the ACMG criteria. Eur J Hum Genet 32, 132 (2024). https://doi.org/10.1038/s41431-023-01288-x

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Published: 31 January 2023
Issue Date: January 2024
DOI: https://doi.org/10.1038/s41431-023-01288-x

Correction: Consensus statement on standards and guidelines for the molecular diagnostics of Alport syndrome: refining the ACMG criteria

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