Rapid therapeutic advances in CFTR modulator science

Cystic fibrosis (CF) is an autosomal recessive genetic disease caused by variants in the gene encoding the cystic fibrosis transmembrane conduction regulator (CFTR) protein. Loss of CFTR function disrupts chloride, bicarbonate and regulation of sodium transport, producing a cascade of mucus obstruct...

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Detalles Bibliográficos
Autor principal: Clancy, John P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Translational Reviews
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6585954/
https://www.ncbi.nlm.nih.gov/pubmed/30289627
http://dx.doi.org/10.1002/ppul.24157

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6585954/
https://www.ncbi.nlm.nih.gov/pubmed/30289627
http://dx.doi.org/10.1002/ppul.24157

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