A large multiexonic genomic deletion within the ALMS1 gene causes Alström syndrome in a consanguineous Pakistani family. Issue 4 (18th August 2015) - Nikopoulos, K.; Butt, G. U.; Farinelli, P.; Mudassar, M.; Domènech‐Estévez, E.; Samara, C.; Kausar, M.; Masroor, I.; Chrast, R.; Rivolta, C.; Siddiqi, S.