Genomic and phenotypic characterization of 404 individuals with neurodevelopmental disorders caused by CTNNB1 variants

Sayaka Kayumi, Luis A Pérez-Jurado, María Palomares, Sneha Rangu, Sarah E Sheppard, Wendy K Chung, Michael C Kruer, Mira Kharbanda, David J Amor, George McGillivray, Julie S Cohen, Sixto García-Miñaúr, Clare L van Eyk, Kelly Harper, Lachlan A Jolly, Dani L Webber, Christopher P Barnett, Fernando Santos-Simarro, Marta Pacio-Míguez, Angela Del PozoSomayeh Bakhtiari, Matthew Deardorff, Holly A Dubbs, Kosuke Izumi, Katheryn Grand, Christopher Gray, Paul R Mark, Elizabeth J Bhoj, Dong Li, Xilma R Ortiz-Gonzalez, Beth Keena, Elaine H Zackai, Ethan M Goldberg, Guiomar Perez de Nanclares, Arrate Pereda, Isabel Llano-Rivas, Ignacio Arroyo, María Ángeles Fernández-Cuesta, Christel Thauvin-Robinet, Laurence Faivre, Aurore Garde, Benoit Mazel, Ange-Line Bruel, Michael L Tress, Eva Brilstra, Amena Smith Fine, Kylie E Crompton, Alexander P A Stegmann, Margje Sinnema, Servi C J Stevens, Joost Nicolai, Gaetan Lesca, Laurence Lion-François, Damien Haye, Nicolas Chatron, Amelie Piton, Mathilde Nizon, Benjamin Cogne, Siddharth Srivastava, Jennifer Bassetti, Candace Muss, Karen W Gripp, Rebecca A Procopio, Francisca Millan, Michelle M Morrow, Melissa Assaf, Andres Moreno-De-Luca, Shelagh Joss, Mark J Hamilton, Marta Bertoli, Nicola Foulds, Shane McKee, Alastair H MacLennan, Jozef Gecz, Mark A Corbett*

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

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Biochemistry, Genetics and Molecular Biology