| Literature DB >> 11448786 |
J J Wine1.
Abstract
The specific effects of some mutations that cause cystic fibrosis suggest that reduced HCO(3)(-) transport is the key to understanding cystic fibrosis pathology. But there is a puzzling discrepancy between measures of CFTR-mediated chloride conductance in expression systems and the sweat chloride values of patients.Entities:
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Year: 2001 PMID: 11448786 DOI: 10.1016/s0960-9822(01)00282-2
Source DB: PubMed Journal: Curr Biol ISSN: 0960-9822 Impact factor: 10.834