A cystic fibrosis patient homozygous for 621 + 1G-->T mutation has a severe pulmonary disease, mild pancreatic insufficiency and a gastro-esophageal reflux. [electronic resource]

By: Contributor(s): Producer: 19970227Description: 149-51 p. digitalISSN:
  • 0009-9163
Subject(s): Online resources: In: Clinical genetics vol. 50
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Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't

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