Monoallelic and biallelic variants in LEF1 are associated with a new syndrome combining ectodermal dysplasia and limb malformations caused by altered WNT signaling

Bibliographic Details
Title: Monoallelic and biallelic variants in LEF1 are associated with a new syndrome combining ectodermal dysplasia and limb malformations caused by altered WNT signaling
Authors: Dufour, William, Alawbathani, Salem, Jourdain, Anne-Sophie, Asif, Maria, Baujat, Geneviève, Becker, Christian, Budde, Birgit, Gallacher, Lyndon, Georgomanolis, Theodoros, Ghoumid, Jamal, Höhne, Wolfgang, Lyonnet, Stanislas, Ba-Saddik, Iman Ali, Manouvrier-Hanu, Sylvie, Motameny, Susanne, Noegel, Angelika A., Pais, Lynn, Vanlerberghe, Clémence, Wagle, Prerana, White, Susan M., Willems, Marjolaine, Nürnberg, Peter, Escande, Fabienne, Petit, Florence, Hussain, Muhammad Sajid
Source: In Genetics in Medicine August 2022 24(8):1708-1721
Database: ScienceDirect
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ISSN:10983600
DOI:10.1016/j.gim.2022.04.022
Published in:Genetics in Medicine
Language:English