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  • publication . Article . Other literature type . 2020
    Open Access
    Publisher: Ovid Technologies (Wolters Kluwer Health)

    Hereditary transthyretin amyloidosis, once a rare progressive neuropathy and/or cardiomyopathy, is now recognized with increasing worldwide frequency, various phenotypes, and over 130 gene mutations identified to date. This inherited disorder develops as a result of mut...

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1 research outcomes, page 1 of 1