| http://www.w3.org/ns/prov#value | - Thus, there are multiple independent lines of evidence suggesting a role of CFTR in normal organogenesis of the lung, intestines, and other organs.Born with more or less normal histology of the lung, pancreas, and liver, but with a more serious intestinal phenotype, CF patients exhibit progressive lung disease largely blamed on decreased mucous hydration [44,45].
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