CFTR Modulators for the Treatment of Cystic Fibrosis.
Year: 2014
Type: article
Abstract: Defects in a single gene lead to the defective proteins that cause cystic fibrosis, making the disease an ideal candidate for mutation-targeted therapy. Although ivacaftor is currently the only FDA-approved CFTR modifier, others are in development.
Source: PubMed Central
Authors: Rebecca S Pettit, Chris Fellner
Language: English
Subfield: Pulmonary and Respiratory Medicine
Field: Medicine
Domain: Health Sciences
Open Access status: green
OpenAlex ID: W1910988217
