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Diversity of the basic defect of homozygous CFTR mutation genotypes in humans
  1. F Stanke1,2,
  2. M Ballmann2,
  3. I Bronsveld4,
  4. T Dörk3,
  5. S Gallati5,
  6. U Laabs1,
  7. N Derichs2,
  8. M Ritzka1,2,
  9. H-G Posselt6,
  10. H K Harms7,
  11. M Griese7,
  12. H Blau8,
  13. G Mastella9,
  14. J Bijman10,
  15. H Veeze11,
  16. B Tümmler1,2
  1. 1
    Klinische Forschergruppe and Abteilungen für
  2. 2
    Pädiatrische Pneumologie und Neonatologie and
  3. 3
    Gynäkologie und Geburtshilfe, Medizinische Hochschule Hannover, Hannover, Germany
  4. 4
    Department of Pulmonology and Tuberculosis, Universitair Medisch Centrum Utrecht, Utrecht, The Netherlands
  5. 5
    Abteilung für Humangenetik, Medizinische Universitätskinderklinik, Inselspital, Universität Bern, Bern, Switzerland
  6. 6
    Universitäts-Kinderklinik, Johann-Wolfgang-Goethe Universität, Frankfurt/Main, Germany
  7. 7
    Dr von Haunersches Kinderspital, Ludwig-Maximilians-Universität, Munich, Germany
  8. 8
    Pulmonary and Cystic Fibrosis Unit, Schneider Children’s Medical Center of Israel, Petah-Tikva, and Sackler School of Medicine, Tel-Aviv University, Tel-Aviv, Israel
  9. 9
    Cystic Fibrosis Center, Ospedale Civile Maggiore, Piazzale Stefani, Verona, Italy
  10. 10
    Erasmus University Rotterdam, Department of Neurosciences, Rotterdam, The Netherlands
  11. 11
    Stichting Diabeter, Rotterdam, The Netherlands
  1. Dr Burkhard Tümmler, Klinische Forschergruppe, OE 6710, Medizinische Hochschule Hannover, Carl-Neuberg-Str. 1, D-30625 Hannover, Germany; tuemmler.burkhard{at}mh-hannover.de

Footnotes

  • Competing interests: None declared.

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Footnotes

  • Competing interests: None declared.

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