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To the Editor:The report by Singer et al1 is elegantly illustrated and provides the practicing clinician with an up-to-date flow chart on how to diagnose amyloidosis as the cause of restrictive cardiomyopathy. However, it is disappointing that the authors did not stress the fact that familial amyloidotic polyneuropathy is an autosomal dominant hereditary form of amyloidosis for …

Restrictive Cardiomyopathy in Familial Amyloidosis TTR-Arg-50