CYLD‐related cutaneous syndrome: variable p.Pro482fs*6 phenotype in five individuals from two unrelated families. (11th August 2020) - Carton de Tournai, D.; Vandernoot, I.; Marangoni, M.; Faverly, D.; Diaz, M.; Casagranda, A.; Berlingin, E.; Van Maldergem, L.