Multiplex epithelium dysfunction due to CLDN10 mutation: the HELIX syndrome

Autor: Hadj-Rabia, Smail, Brideau, Gaelle, Al-Sarraj, Yasser, Maroun, Rachid C., Figueres, Marie-Lucile, Leclerc-Mercier, Stéphanie, Olinger, Eric, Baron, Stéphanie, Chaussain, Catherine, Nochy, Dominique, Taha, Rowaida Z., Knebelmann, Bertrand, Joshi, Vandana, Curmi, Patrick A., Kambouris, Marios, Vargas-Poussou, Rosa, Bodemer, Christine, Devuyst, Olivier, Houillier, Pascal, El-Shanti, Hatem
Zdroj: In Genetics in Medicine February 2018 20(2):190-201
Databáze: ScienceDirect
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