A case of transthyretin amyloidosis with myopathy, neuropathy, and cardiomyopathy resulting from an exceedingly rare mutation transthyretin Ala120Ser (c.418G > T, p.Ala140Ser). (3rd July 2018) - Patel, Kavisha; Tagoe, Clement; Bieri, Phyllis; Weidenheim, Karen; Tauras, James M.