A familial case of Keratitis-Ichthyosis-Deafness (KID) syndrome with the GJB2 mutation G45E
Laurence Jonard(Inserm), S. Hadj‐Rabia(Hôpital Necker-Enfants Malades), Sylvie Freitag(Hôpital Necker-Enfants Malades), Christine Bodemer(Hôpital Necker-Enfants Malades), Françoise Denoyelle(Hôpital Necker-Enfants Malades), M’hamed Grati(University of Miami), Christophe Parsy(Hôpital Necker-Enfants Malades), Delphine Feldmann(Hôpital Armand-Trousseau), Rémy Couderc(Sorbonne Université), Céleste Koval(Inserm), Martine Sinico(Hôpital Intercommunal de Créteil), Sandrine Marlin(Hôpital Necker-Enfants Malades)
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