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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 Williams
    • Andrew 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

Research output: Contribution to journal › Article › peer-review

72   Link opens in a new tab Scopus citations

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Medicine and Dentistry

Biochemistry, Genetics and Molecular Biology

Immunology and Microbiology