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Cystic fibrosis transmembrane conductance regulator protein repair as a therapeutic strategy in cystic fibrosis

PURPOSE OF REVIEW: Recent progress in understanding the production, processing, and function of the cystic fibrosis gene product, the cystic fibrosis transmembrane conductance regulator (CFTR), has revealed new therapeutic targets to repair the mutant protein. Classification of CFTR mutations and ne...

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Detalhes bibliográficos
Main Authors: Sloane, Peter A., Rowe, Steven M.
Formato: Artigo
Idioma:Inglês
Publicado em: 2010
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3733473/
https://ncbi.nlm.nih.gov/pubmed/20829696
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/MCP.0b013e32833f1d00
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