A case of transthyretin amyloidosis with myopathy, neuropathy, and cardiomyopathy resulting from an exceedingly rare mutation transthyretin Ala120Ser (c.418G > T, p.Ala140Ser)

Kavisha Patel, Clement Tagoe, Phyllis Bieri, Karen Weidenheim, James M. Tauras

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