Multiplex epithelium dysfunction due to CLDN10 mutation: the HELIX syndrome.

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.
Genet Med; 20(2): 190-201, 2018 02.
Artigo em Inglês | MEDLINE | ID: mdl-28771254