Mutations of IFT81, encoding an IFT-B core protein, as a rare cause of a ciliopathy. Issue 1 (December 2015) - Perrault, I; Halbritter, J; Porath, J; Gerard, X; Braun, D; Gee, H; Fathy, H; Saunier, S; Cormier-Daire, V; Thomas, S; Attié-Bitach, T; Boddaert, N; et al.