CFTR with a partially deleted R domain corrects the cystic fibrosis chloride transport defect in human airway epithelia in vitro and in mouse nasal mucosa in vivo.

Source:http://linkedlifedata.com/resource/pubmed/id/11854474

Proc. Natl. Acad. Sci. U.S.A. 2002 Mar 5 99 5 3093-8

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PMID
11854474