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