Corrigendum to "ATP7B variant spectrum in a French pediatric Wilson disease cohort" [Eur. J. Med. Genet. 64 (10) (October 2021) 104305]

Eduardo Couchonnal¹, Sophie Bouchard², Thomas Damgaard Sandahl³, Cecile Pagan⁴, Laurence Lion-François⁵, Olivier Guillaud⁵, Dalila Habes⁶, Dominique Debray⁷, Thierry Lamireau⁸, Pierre Broué⁹, Alexandre Fabre¹⁰, Claire Vanlemmens¹¹, Rodolphe Sobesky¹², Frederic Gottrand¹³, Laure Bridoux-Henno¹⁴, Abdelouahed Belmalih⁵, Aurelia Poujois¹⁵, Corinne Collet¹⁶, Bruno Francou¹⁷, Anne Sophie Brunet¹⁸, Alain Lachaux¹⁹, Micheline Misrahi²⁰, Muriel Bost²¹

Affiliations

¹ Hospices Civils de Lyon, National Center for Wilson's Disease and Department of Pediatric Gastroenterology, Hepatology and Nutrition Children's Hospital of Lyon, France; European Reference Network on Hepatological Diseases (ERN RARE-LIVER), Germany. Electronic address: eduardo.couchonnal-bedoya@chu-lyon.fr.
² Claude Bernard Lyon 1 University Lyon, France.
³ European Reference Network on Hepatological Diseases (ERN RARE-LIVER), Germany; Department of Hepatology and Gastroenterology, Aarhus University Hospital, Aarhus N, Denmark.
⁴ Department of Biochemistry and Molecular Biology, LBMMS, Hospices Civils de Lyon, France.
⁵ Hospices Civils de Lyon, National Center for Wilson's Disease and Department of Pediatric Gastroenterology, Hepatology and Nutrition Children's Hospital of Lyon, France; European Reference Network on Hepatological Diseases (ERN RARE-LIVER), Germany.
⁶ European Reference Network on Hepatological Diseases (ERN RARE-LIVER), Germany; Pediatric Hepatology and Liver Transplantation Unit, National Reference Centre for Biliary Atresia and Genetic Cholestasis, FILFOIE, ERN RARE LIVER, Bicêtre Hospital, Assistance Publique - Hôpitaux de Paris, Le Kremlin-Bicêtre, France.
⁷ European Reference Network on Hepatological Diseases (ERN RARE-LIVER), Germany; Pediatric Hepatology Unit, Reference Center for Biliary Atresia and Genetic Cholestasis, Hôpital Necker-Enfants Malades, AP-HP, Université Paris Centre, Paris, France.
⁸ Children's Hospital, Paediatric Gastroenterology Unit, Bordeaux, France.
⁹ Children University Hospital, Metabolic Disease Department, Toulouse, France.
¹⁰ APH, Timone Enfant, Service de Pédiatrie Multidisciplinaire, Marseille, France; Aix Marseille Univ, INSERM, MMG, Marseille, France.
¹¹ University Hospital of Besancon, Paediatric Gastroenterology Unit, Besacon, France.
¹² European Reference Network on Hepatological Diseases (ERN RARE-LIVER), Germany; Paul Brousse Hospital, Hepatobiliary Centre, Hepatobiliary Centre, France; French National Rare Disease Competence Centre "Wilson's Disease and Other Copper-related Rare Diseases", Paul Brousse Hospital, 94800, Villejuif, France.
¹³ Univ- Lille, CHU Lille, UMR1286 Department of Pediatric Gastroenterology Hepatology and Nutrition, Lille, France.
¹⁴ CHU Rennes, Department of Pediatric Gastroenterology, Rennes, France.
¹⁵ European Reference Network on Hepatological Diseases (ERN RARE-LIVER), Germany; French National Rare Disease Reference Centre "Wilson's Disease and Other Copper-related Rare Diseases", Rothschild Foundation Hospital, Neurology Department, Paris, France.
¹⁶ Department of Biochemistry and Molecular Biology, Lariboisiere University Hospital, APHP, Paris, France.
¹⁷ Université Paris Saclay, Faculté de Médecine, Department of Molecular Genetics of Metabolic and Reproductive Diseases, Hôpital Bicêtre, Assistance Publique-Hôpitaux de Paris, AP-HP, Hôpitaux Universitaires Paris-Saclay, 94275, Le Kremlin-Bicêtre, France.
¹⁸ Hospices Civils de Lyon, National Center for Wilson's Disease and Department of Pediatric Gastroenterology, Hepatology and Nutrition Children's Hospital of Lyon, France.
¹⁹ Hospices Civils de Lyon, National Center for Wilson's Disease and Department of Pediatric Gastroenterology, Hepatology and Nutrition Children's Hospital of Lyon, France; European Reference Network on Hepatological Diseases (ERN RARE-LIVER), Germany; Claude Bernard Lyon 1 University Lyon, France.
²⁰ French National Rare Disease Competence Centre "Wilson's Disease and Other Copper-related Rare Diseases", Paul Brousse Hospital, 94800, Villejuif, France; Université Paris Saclay, Faculté de Médecine, Department of Molecular Genetics of Metabolic and Reproductive Diseases, Hôpital Bicêtre, Assistance Publique-Hôpitaux de Paris, AP-HP, Hôpitaux Universitaires Paris-Saclay, 94275, Le Kremlin-Bicêtre, France; UMR-S 1193 INSERM - Université Paris Saclay, Faculté de Medecine, Hôpital Paul Brousse, 94800, Villejuif, France.
²¹ Hospices Civils de Lyon, National Center for Wilson's Disease and Department of Pediatric Gastroenterology, Hepatology and Nutrition Children's Hospital of Lyon, France; European Reference Network on Hepatological Diseases (ERN RARE-LIVER), Germany; Department of Biochemistry and Molecular Biology, LBMMS, Hospices Civils de Lyon, France.

PMID: 35183456
DOI: 10.1016/j.ejmg.2022.104453

Published Erratum

Corrigendum to "ATP7B variant spectrum in a French pediatric Wilson disease cohort" [Eur. J. Med. Genet. 64 (10) (October 2021) 104305]

Eduardo Couchonnal et al. Eur J Med Genet. 2022 Mar.

. 2022 Mar;65(3):104453.

doi: 10.1016/j.ejmg.2022.104453. Epub 2022 Feb 16.

Authors

Affiliations

¹ Hospices Civils de Lyon, National Center for Wilson's Disease and Department of Pediatric Gastroenterology, Hepatology and Nutrition Children's Hospital of Lyon, France; European Reference Network on Hepatological Diseases (ERN RARE-LIVER), Germany. Electronic address: eduardo.couchonnal-bedoya@chu-lyon.fr.
² Claude Bernard Lyon 1 University Lyon, France.
³ European Reference Network on Hepatological Diseases (ERN RARE-LIVER), Germany; Department of Hepatology and Gastroenterology, Aarhus University Hospital, Aarhus N, Denmark.
⁴ Department of Biochemistry and Molecular Biology, LBMMS, Hospices Civils de Lyon, France.
⁵ Hospices Civils de Lyon, National Center for Wilson's Disease and Department of Pediatric Gastroenterology, Hepatology and Nutrition Children's Hospital of Lyon, France; European Reference Network on Hepatological Diseases (ERN RARE-LIVER), Germany.
⁶ European Reference Network on Hepatological Diseases (ERN RARE-LIVER), Germany; Pediatric Hepatology and Liver Transplantation Unit, National Reference Centre for Biliary Atresia and Genetic Cholestasis, FILFOIE, ERN RARE LIVER, Bicêtre Hospital, Assistance Publique - Hôpitaux de Paris, Le Kremlin-Bicêtre, France.
⁷ European Reference Network on Hepatological Diseases (ERN RARE-LIVER), Germany; Pediatric Hepatology Unit, Reference Center for Biliary Atresia and Genetic Cholestasis, Hôpital Necker-Enfants Malades, AP-HP, Université Paris Centre, Paris, France.
⁸ Children's Hospital, Paediatric Gastroenterology Unit, Bordeaux, France.
⁹ Children University Hospital, Metabolic Disease Department, Toulouse, France.
¹⁰ APH, Timone Enfant, Service de Pédiatrie Multidisciplinaire, Marseille, France; Aix Marseille Univ, INSERM, MMG, Marseille, France.
¹¹ University Hospital of Besancon, Paediatric Gastroenterology Unit, Besacon, France.
¹² European Reference Network on Hepatological Diseases (ERN RARE-LIVER), Germany; Paul Brousse Hospital, Hepatobiliary Centre, Hepatobiliary Centre, France; French National Rare Disease Competence Centre "Wilson's Disease and Other Copper-related Rare Diseases", Paul Brousse Hospital, 94800, Villejuif, France.
¹³ Univ- Lille, CHU Lille, UMR1286 Department of Pediatric Gastroenterology Hepatology and Nutrition, Lille, France.
¹⁴ CHU Rennes, Department of Pediatric Gastroenterology, Rennes, France.
¹⁵ European Reference Network on Hepatological Diseases (ERN RARE-LIVER), Germany; French National Rare Disease Reference Centre "Wilson's Disease and Other Copper-related Rare Diseases", Rothschild Foundation Hospital, Neurology Department, Paris, France.
¹⁶ Department of Biochemistry and Molecular Biology, Lariboisiere University Hospital, APHP, Paris, France.
¹⁷ Université Paris Saclay, Faculté de Médecine, Department of Molecular Genetics of Metabolic and Reproductive Diseases, Hôpital Bicêtre, Assistance Publique-Hôpitaux de Paris, AP-HP, Hôpitaux Universitaires Paris-Saclay, 94275, Le Kremlin-Bicêtre, France.
¹⁸ Hospices Civils de Lyon, National Center for Wilson's Disease and Department of Pediatric Gastroenterology, Hepatology and Nutrition Children's Hospital of Lyon, France.
¹⁹ Hospices Civils de Lyon, National Center for Wilson's Disease and Department of Pediatric Gastroenterology, Hepatology and Nutrition Children's Hospital of Lyon, France; European Reference Network on Hepatological Diseases (ERN RARE-LIVER), Germany; Claude Bernard Lyon 1 University Lyon, France.
²⁰ French National Rare Disease Competence Centre "Wilson's Disease and Other Copper-related Rare Diseases", Paul Brousse Hospital, 94800, Villejuif, France; Université Paris Saclay, Faculté de Médecine, Department of Molecular Genetics of Metabolic and Reproductive Diseases, Hôpital Bicêtre, Assistance Publique-Hôpitaux de Paris, AP-HP, Hôpitaux Universitaires Paris-Saclay, 94275, Le Kremlin-Bicêtre, France; UMR-S 1193 INSERM - Université Paris Saclay, Faculté de Medecine, Hôpital Paul Brousse, 94800, Villejuif, France.
²¹ Hospices Civils de Lyon, National Center for Wilson's Disease and Department of Pediatric Gastroenterology, Hepatology and Nutrition Children's Hospital of Lyon, France; European Reference Network on Hepatological Diseases (ERN RARE-LIVER), Germany; Department of Biochemistry and Molecular Biology, LBMMS, Hospices Civils de Lyon, France.

PMID: 35183456
DOI: 10.1016/j.ejmg.2022.104453

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Erratum for

ATP7B variant spectrum in a French pediatric Wilson disease cohort.
Couchonnal E, Bouchard S, Sandahl TD, Pagan C, Lion-François L, Guillaud O, Habes D, Debray D, Lamireau T, Broué P, Fabre A, Vanlemmens C, Sobesky R, Gottrand F, Bridoux-Henno L, Belmalih A, Poujois A, Brunet AS, Lachaux A, Bost M. Couchonnal E, et al. Eur J Med Genet. 2021 Oct;64(10):104305. doi: 10.1016/j.ejmg.2021.104305. Epub 2021 Aug 13. Eur J Med Genet. 2021. PMID: 34400371

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Corrigendum to "ATP7B variant spectrum in a French pediatric Wilson disease cohort" [Eur. J. Med. Genet. 64 (10) (October 2021) 104305]

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Corrigendum to "ATP7B variant spectrum in a French pediatric Wilson disease cohort" [Eur. J. Med. Genet. 64 (10) (October 2021) 104305]

Authors

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Erratum for

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