Monoallelic and biallelic variants in LEF1 are associated with a new syndrome combining ectodermal dysplasia and limb malformations caused by altered WNT signaling
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Published:2022-08
Issue:8
Volume:24
Page:1708-1721
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ISSN:1098-3600
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Container-title:Genetics in Medicine
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language:en
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Short-container-title:Genetics in Medicine
Author:
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 FlorenceORCID,
Hussain Muhammad Sajid
Subject
Genetics (clinical)
Cited by
4 articles.
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