Heterozygous mutations in the C-terminal domain of COPA underlie a complex autoinflammatory syndrome von Delafontaine, Selket, Lannuzzo, Alberto, Bigley, Tarin M, Mylemans, Bram, Rana, Ruchit, Baatsen, Pieter, Poli, Maria Cecilia, Rymen, Daisy, Jansen, Katrien, Mekahli, Djalila, Casteels, Ingele, Cassiman, Catherine, Demaerel, Philippe, Lepelley, Alice, Frémond, Marie-Louise, Schrijvers, Rik, Bossuyt, Xavier, Vints, Katlijn, Huybrechts, Wim, Tacine, Rachida, Willekens, Karen, Corveleyn, Anniek, Boeckx, Bram, Baggio, Marco, Ehlers, Lisa, Munck, Sebastian, Lambrechts, Diether, Voet, Arnout, Moens, Leen, Bucciol, Giorgia, Cooper, Megan A, Davis, Carla M, Delon, Jérôme, Meyts, Isabelle

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