Björkenheim, A., Szabó, B., & Sztaniszláv, Á. J. (2020). Hereditary transthyretin amyloidosis caused by the rare Phe33Leu mutation. BMJ Case Rep.
Citação norma ChicagoBjörkenheim, Anna, Barna Szabó, and Áron József Sztaniszláv. "Hereditary Transthyretin Amyloidosis Caused By the Rare Phe33Leu Mutation." BMJ Case Rep 2020.
MLA CitationBjörkenheim, Anna, Barna Szabó, and Áron József Sztaniszláv. "Hereditary Transthyretin Amyloidosis Caused By the Rare Phe33Leu Mutation." BMJ Case Rep 2020.
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