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However, the etiology of PF remains elusive in the majority of patients and is classified as idiopathic pulmonary fibrosis (IPF), characterized by progressive exacerbation of dyspnea, persistent dry cough, restrictive ventilation dysfunction, and ultimately culminating in respiratory failure-induced mortality [2, 3]
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CroftPAltmanDGDeeksJJDunnKMHayADHemingwayHet al
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