Author:
Poller W.,Faber J. -P.,Scholz S.,Olek K.,Müller K. -M.
Publisher
Springer Science and Business Media LLC
Subject
General Medicine,Genetics (clinical),Drug Discovery,Molecular Medicine
Reference35 articles.
1. Boat TF, Walsh MJ, Beaudet AL (1989) Cystic fibrosis. In: Scriver CR, Beaudet AI, Sly WS, Valle D (eds) The metabolic basis of inherited disease. McGraw-Hill, New York
2. Cutting GR, Kasch LM, Rosenstein BJ, Zielenski J, Tsui L-C, Antonarakis SE, Kazazian HH (1990a) A cluster of cystic fibrosis mutations in the first nucleotide-binding fold of the cystic fibrosis conductance regulator protein. Nature 346:366–369
3. Cutting GR, Kasch LM, Rosenstein BJ, Tsui L-C, Kazazian HH, Antonarakis SE (1990b) Two patients with cystic fibrosis, nonsense mutations in each cystic fibrosis gene, and mild pulmonary disease. N Engl J Med 323:1685–1689
4. Davies K (1990) Cystic fibrosis — complementary endeavours. Nature 348:110–111
5. Davis PB, Hubbard VS, Sant'Agnese PA (1980) Low sweat electrolytes in a patient with cystic fibrosis. Am J Med 69:643–646
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