- Titre
- Monoallelic and biallelic variants in LEF1 are associated with a new syndrome combining ectodermal dysplasia and limb malformations caused by altered WNT signaling
- Créateurs - sans rôle
- William Dufour - Centre Hospitalier Universitaire de LilleSalem Alawbathani - University of CologneAnne-Sophie JourdainMaria Asif - University of CologneGeneviève Baujat - Hôpital Necker-Enfants MaladesChristian Becker - University Hospital CologneBirgit Budde - University of CologneLyndon Gallacher - The University of MelbourneTheodoros Georgomanolis - University Hospital CologneJamal Ghoumid - Centre Hospitalier Universitaire de LilleWolfgang Höhne - University Hospital CologneStanislas Lyonnet - Hôpital Necker-Enfants MaladesIman Ali Ba-Saddik - University of AdenSylvie Manouvrier-Hanu - Centre Hospitalier Universitaire de LilleSusanne Motameny - University Hospital CologneAngelika Noegel - University of CologneLynn Pais - Broad InstituteClémence Vanlerberghe - Centre Hospitalier Universitaire de LillePrerana Wagle - Cologne Excellence Cluster on Cellular Stress Responses in Aging Associated DiseasesSusan White - Victorian Clinical Genetics ServicesMarjolaine Willems - Université de Montpellier, Institut des Neurosciences de Montpellier - INMPeter Nürnberg - University of CologneFabienne Escande - Centre Hospitalier Universitaire de LilleFlorence Petit - Université de LilleMuhammad Sajid Hussain - University Hospital Cologne
- Détails de publication
- Genetics in Medicine, Vol.24(8), pp.1708-1721
- Identifiants
- 99153117809311
- Unité académique
- Institut des Neurosciences de Montpellier - INM
- Langue
- English
- Type de ressource
- Journal article
- Champs locaux
- hal-04943538
Article de revue
Monoallelic and biallelic variants in LEF1 are associated with a new syndrome combining ectodermal dysplasia and limb malformations caused by altered WNT signaling
Genetics in Medicine, Vol.24(8), pp.1708-1721
08/2022
Indicateurs
1 Consultations de la notice