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Given that pulmonary fibrosis is characterized by a progressive pulmonary functional decline (Behr, 2013), studies seeking safe and effective treatments for pulmonary fibrosis are a crucial priority

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Similar content being viewed by others Introduction Transthyretin (TTR) amyloidosis (ATTR) is a progressive, life-threatening disorder characterized by the extracellular deposition of amyloid fibrils derived from the TTR protein [1]

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