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A TP63 Mutation Causes Prominent Alopecia with Mild Ectodermal Dysplasia

Sabine Duchatelet 1, 2 Claudia Russo 3 Christian Osterburg 4 Stéphanie Mallet 5 Christine Bole-Feysot 6 Patrick Nitschke 7 Marie-Aleth Richard 5 Volker Dötsch 4 Caterina Missero 3 Aude Nassif 8 Alain Hovnanian 1, 9 
1 Equipe Inserm U1163 - Genetic skin diseases : from disease mechanism to therapies
IMAGINE - U1163 - Imagine - Institut des maladies génétiques
2 UPD5 - Université Paris Descartes - Paris 5
3 University of Naples Federico II
4 Goethe-University Frankfurt am Main
5 CEReSS - Centre d'études et de recherche sur les services de santé et la qualité de vie
6 Plateforme de génomique [SFR Necker]
SFR Necker - UMS 3633 / US24 - Structure Fédérative de Recherche Necker
7 BIP-D - Plate Forme Paris Descartes de Bioinformatique
8 CMIP - Centre Médical de l'Institut Pasteur
9 CHU Necker - Enfants Malades [AP-HP] - Département de Génétique
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Submitted on : Sunday, April 19, 2020 - 7:06:19 PM
Last modification on : Thursday, October 20, 2022 - 3:10:07 PM

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INSERM | PASTEUR | CNRS | UNIV-AMU | UNIV-PARIS | UP-SANTE

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Sabine Duchatelet, Claudia Russo, Christian Osterburg, Stéphanie Mallet, Christine Bole-Feysot, et al.. A TP63 Mutation Causes Prominent Alopecia with Mild Ectodermal Dysplasia. Journal of Investigative Dermatology, 2020, ⟨10.1016/j.jid.2019.06.154⟩. ⟨pasteur-02547254⟩

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