Hereditary transthyretin amyloidosis caused by the rare Phe33Leu mutation | BMJ Case Reports

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Hereditary transthyretin amyloidosis caused by the rare Phe33Leu mutation

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Cite this article as:: Björkenheim A, Szabó B, Sztaniszláv ÁJ

Hereditary transthyretin amyloidosis caused by the rare Phe33Leu mutation

BMJ Case Reports CP 2020;13:e232756.