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Idiopathic pulmonary fibrosis (IPF) is the most common and severe form of lung disease characterized by relentless scarring leading to death within an average of four years from the time of diagnosis.

United statesBoston universityDarrell kottonDavidc seldinMichaelf beersDavida cooperKontantinos alysandratosEmily hendersonRobertl mayockBu boston medical centerUniversity of pennsylvania perelman school medicineUniversity of pennsylvaniaBoston university school of medicineBoston university schoolCorresponding authorBoston medical center