https://www.selleckchem.com/products/EX-527.html
Idiopathic pulmonary fibrosis (IPF) is a progressive fibrosing interstitial lung disease (ILD). This prospective observational study aimed at the evaluation of any correlation between genetic variants associated with IPF susceptibility and high-resolution computed tomography (HRCT) patterns. It also aimed at evidencing any differences in the HRTC pattern between the familial and sporadic form at diagnosis and after two years. A total of 65 IPF patients (mean age at diagnosis 65 ± 1 were enrolled after having given written informed cons
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