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[The identification of the cystic fibrosis gene and its product, cystic fibrosis transmembrane conductance regulator (CFTR), has widened the spectrum of the disease from the classical case of the infant with cystic fibrosis to the elderly childless man with unexplained bronchiectasis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
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