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Transthyretin amyloid cardiomyopathy (ATTR-CM) is an inexorably progressive and ultimately fatal cardiomyopathy characterized by the deposition of misfolded transthyretin (TTR) in the form of amyloid fibrils within the myocardium.1 Transthyretin amyloid (ATTR) fibrils are insoluble protease–resistant beta-pleated sheets that are stabilized within the extracellular matrix, disrupting the integrity, structure and function of the myocardium.2Â ATTR-amyloid fibril […]
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