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Telomere Dysfunction in Idiopathic Pulmonary Fibrosis

11 Nov 2021

Abstract excerpt

Idiopathic pulmonary fibrosis is an age-dependent progressive and fatal lung disease of unknown etiology, which is characterized by the excessive accumulation of extracellular matrix inside the interstitial layer of the lung parenchyma that leads to abnormal scar architecture and compromised lung function capacity. Recent genetic studies have attributed the pathological genes or genetic mutations associated with...

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Share to Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
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PMID: 34859008
DOI: 10.3389/fmed.2021.739810

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