A novel compound heterozygous mutation of C20orf54 gene associated with Brown–Vialetto–Van Laere syndrome in an Italian family. Issue 7 (10th June 2013) - Bandettini di Poggio, M.; Gagliardi, S.; Pardini, M.; Marchioni, E.; Monti Bragadin, M.; Reni, L.; Doria‐Lamba, L.; Roccatagliata, L.; Ceroni, M.; Schenone, A.; Cereda, C.