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)
Publication date
2024-08
Authors
Layo-Carris, Dana E.
Lubin, Emily E.
Sangree, Annabel K.
Clark, Kelly J.
Durham, Emily L.
Gonzalez, Elizabeth M.
Smith, Sarina
Angireddy, Rajesh
Wang, Xiao Min
Weiss, Erin
Editors
Advisors
Supervisors
Document Type
Comment
Metadata
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cc_by
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.
Keywords
Genetics, Genetics(clinical)
Citation
Layo-Carris, D E, Lubin, E E, Sangree, A K, Clark, K J, Durham, E L, Gonzalez, E M, Smith, S, Angireddy, R, Wang, X M, 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, A I, Nowaczyk, M J M, Hančárová, M, Bendová, Š, Prchalova, D, Sedláček, Z, Baxová, A, Nowak, C B, Douglas, J, Chung, W K, Longo, N, Platzer, K, Klöckner, C, Averdunk, L, Wieczorek, D, Krey, I, Zweier, C, Reis, A, Balci, T, Simon, M, Kroes, H Y, Wiesener, A, Vasileiou, G, Marinakis, N M, Veltra, D, Sofocleous, C, Kosma, K, Synodinos, J T, Voudris, K A, Vuillaume, M L, Gueguen, P, Derive, N, Colin, E, Battault, C, Au, B, Delatycki, M, Wallis, M, Gallacher, L, Majdoub, F, Smal, N, Weckhuysen, S, Schoonjans, A S, Kooy, R F, Meuwissen, M, Cocanougher, B T, Taylor, K, Pizoli, C E, McDonald, M T, James, P, Roeder, E R, Littlejohn, R, Borja, N A, Thorson, W, King, K, Stoeva, R, Suerink, M, Nibbeling, E, Baskin, S, Guyader, G L E, Kaplan, J, Muss, C, Carere, D A, Bhoj, E J K & 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, vol. 32, no. 8, 1032. https://doi.org/10.1038/s41431-024-01659-y