Artwork for Pathophysiology and Clinical Features of TTR Cardiac Amyloidosis: No Longer a “Rare” Disease and Still Underdiagnosed
Closing Knowledge Gaps in Transthyretin Cardiomyopathy (ATTR-CM)

Pathophysiology and Clinical Features of TTR Cardiac Amyloidosis: No Longer a “Rare” Disease and Still Underdiagnosed
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