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Hereditary systemic amyloidosis caused by K19T apolipoprotein C-II variant.

TitleHereditary systemic amyloidosis caused by K19T apolipoprotein C-II variant.
Publication TypeJournal Article
Year of Publication2019
AuthorsLiapis, K., Panagopoulou P., Charitaki E., Rowczenio D., Gilbertson J., Papathoma A., Kostopoulou M., Dimopoulos M. A., Gillmore J. D., & Kastritis E.
JournalAmyloid
Volume26
Issue1
Pagination52-53
Date Published2019 Mar
ISSN1744-2818
KeywordsAged, 80 and over, Amyloidosis, Familial, Apolipoprotein C-II, Humans, Male, Mutation
DOI10.1080/13506129.2018.1562442
Alternate JournalAmyloid
PubMed ID30686043

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