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The Cystic Fibrosis Intestine

The clinical manifestations of cystic fibrosis (CF) result from dysfunction of the cystic fibrosis transmembrane regulator protein (CFTR). The majority of people with CF have a limited life span as a consequence of CFTR dysfunction in the respiratory tract. However, CFTR dysfunction in the gastroint...

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Detalhes bibliográficos
Main Authors: De Lisle, Robert C., Borowitz, Drucy
Formato: Artigo
Idioma:Inglês
Publicado em: Cold Spring Harbor Laboratory Press 2013
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3753720/
https://ncbi.nlm.nih.gov/pubmed/23788646
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1101/cshperspect.a009753
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