Cystic fibrosis patients bearing both the common missense mutation gly→asp at codon 551 and the ΔF508 mutation are clinically indistinguishable from ΔF508 homozygotes, except for decreased risk of meconium ileus
Ada Hamosh, Terri M. King, Beryl J. Rosenstein, Mary Corey, Henry Levison, Peter Durie, Lap Chee Tsui, Iain McIntosh, Marion Keston, David J.H. Brock, Milan Macek, Dana Zemková, Hana Krásničanová, Věra Vávrová, Milan Macek, Neil Golder, Martin J. Schwarz, Maurice Super, Eila K. Watson, Carolyn WilliamsAndrew Bush, Sinead M. O'Mahoney, Peter Humphries, Miguel A. DeArce, André Reis, Joachim Bürger, Manfred Stuhrmann, Jörg Schmidtke, Ulrich Wulbrand, Thilo Dörk, Burkhard Tümmler, Garry R. Cutting
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