Correction: Expanded phenotypic spectrum of neurodevelopmental and neurodegenerative disorder Bryant-Li-Bhoj syndrome with 38 additional individuals (European Journal of Human Genetics, (2024), 32, 8, (928-937), 10.1038/s41431-024-01610-1)

Layo-Carris DE, Lubin EE, Sangree AK, Clark KJ, Durham EL, Gonzalez EM, Smith S, Angireddy R, Wang XM, Weiss E, Toutain A, Mendoza-Londono R, Dupuis L, Damseh N, Velasco D, Valenzuela I, Codina-Solà M, Ziats C, Have J, Clarkson K, Steel D, Kurian M, Barwick K, Carrasco D, Dagli AI, Nowaczyk MJ, Hančárová M, Bendová Š, Prchalova D, Sedláček Z, Baxová A, Nowak CB, Douglas J, Chung WK, Longo N, Platzer K, Klöckner C, Averdunk L, Wieczorek D, Krey I, Zweier C, Reis A, Balci T, Simon M, Kroes HY, Wiesener A, Vasileiou G, Marinakis NM, Veltra D, Sofocleous C, Kosma K, Synodinos JT, Voudris KA, Vuillaume ML, Gueguen P, Derive N, Colin E, Battault C, Au B, Delatycki M, Wallis M, Gallacher L, Majdoub F, Smal N, Weckhuysen S, Schoonjans AS, Kooy RF, Meuwissen M, Cocanougher BT, Taylor K, Pizoli CE, McDonald MT, James P, Roeder ER, Littlejohn R, Borja NA, Thorson W, King K, Stoeva R, Suerink M, Nibbeling E, Baskin S, Guyader GL, Kaplan J, Muss C, Carere DA, Bhoj EJ, Bryant LM (2024)

Publication Type: Journal article, Erratum

Publication year: 2024

Journal

Book Volume: 32

Pages Range: 1032-

Journal Issue: 8

DOI: 10.1038/s41431-024-01659-y

Abstract

An author was not named. The missing author is: “Annick Toutain” Her affiliation is: 27 Service de Génétique, CHU de Tours, Tours, France. 28 UMR1253, iBrain, Inserm, University of Tours, Tours, France.

Authors with CRIS profile

Involved external institutions

National and Kapodistrian University of Athens Greece (GR) Children's Hospital of Philadelphia United States (USA) (US) Centre Hospitalier Régional Universitaire de Tours France (FR) The Hospital for Sick Children (SickKids) Canada (CA) University of Nebraska Medical Center (UNMC) United States (USA) (US) Vall d'Hebron University Hospital / Hospital Universitari Vall d'Hebron Spain (ES) Shodair Children's Hospital United States (USA) (US) Greenwood Genetic Center United States (USA) (US) University College London (UCL) United Kingdom (GB) Cook Children's Medical Center United States (USA) (US) GCS SeqOIA France (FR) Orlando Health Arnold Palmer Hospital for Children United States (USA) (US) Centre hospitalier universitaire (CHU) d'Angers France (FR) Hamilton Health Sciences (HHS) Canada (CA) Univerzita Karlova v Praze / Charles University in Prague Czech Republic (CZ) Universität Leipzig Germany (DE) Murdoch Childrens Research Institute Australia (AU) Tasmanian Department of Health Australia (AU) Nemours Children's Hospital United States (USA) (US) Massachusetts General Hospital United States (USA) (US) Veterans Affairs Healthcare System Boston and Harvard Medical School United States (USA) (US) University of Utah United States (USA) (US) Flanders Institute for Biotechnology / Vlaams Instituut voor Biotechnologie (VIB) Belgium (BE) Heinrich-Heine-Universität Düsseldorf Germany (DE) Western University Canada (CA) University Medical Centre Utrecht (UMC Utrecht) Netherlands (NL) Hospital Network Antwerp / Ziekenhuis Netwerk Antwerpen (ZNA) Belgium (BE) Duke University Health System United States (USA) (US) DMG Children's Rehabilitative Services United States (USA) (US) Baylor College of Medicine United States (USA) (US) University of Miami United States (USA) (US) Multicare Health System United States (USA) (US) Centre Hospitalier Le Mans France (FR) Leiden University Medical Center Netherlands (NL) University of Calgary Canada (CA) General University Hospital in Prague / Všeobecná Fakultní Nemocnice v Praze (VFN) Czech Republic (CZ) Centre hospitalier universitaire de Poitiers (CHU de Poitiers) France (FR) GeneDX United States (USA) (US)

How to cite

APA:

Layo-Carris, D.E., Lubin, E.E., Sangree, A.K., Clark, K.J., Durham, E.L., Gonzalez, E.M.,... Bryant, L.M. (2024). Correction: Expanded phenotypic spectrum of neurodevelopmental and neurodegenerative disorder Bryant-Li-Bhoj syndrome with 38 additional individuals (European Journal of Human Genetics, (2024), 32, 8, (928-937), 10.1038/s41431-024-01610-1). European Journal of Human Genetics, 32(8), 1032-. https://doi.org/10.1038/s41431-024-01659-y

MLA:

Layo-Carris, Dana E., et al. "Correction: Expanded phenotypic spectrum of neurodevelopmental and neurodegenerative disorder Bryant-Li-Bhoj syndrome with 38 additional individuals (European Journal of Human Genetics, (2024), 32, 8, (928-937), 10.1038/s41431-024-01610-1)." European Journal of Human Genetics 32.8 (2024): 1032-.

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