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

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

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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