ISSN:
1546-170X
Source:
Nature Archives 1869 - 2009
Topics:
Biology
,
Medicine
Notes:
[Auszug] To the editor — The most direct strategy for treating the respiratory manifestations of cystic fibrosis (CF) is in vivo gene therapy, in which the normal human CF transmembrane conductance regulator (CFTR) cDNA is transferred to the airway epithelium, where it can express the CFTR protein and ...
Type of Medium:
Electronic Resource
URL:
http://dx.doi.org/10.1038/nm0395-182b
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