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

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http://dx.doi.org/10.1080/13506129.2018.1491398DOI Listing

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