Treatment of volanesorsen in a patient with familial chylmicronaemia syndrome (FCS) due to homozygous c.337T>C(p.TRP113ARG) - mutation and impact of dietary incompliance: A case report. (August 2022)

Record Type:: Journal Article
Title:: Treatment of volanesorsen in a patient with familial chylmicronaemia syndrome (FCS) due to homozygous c.337T>C(p.TRP113ARG) - mutation and impact of dietary incompliance: A case report. (August 2022)
Main Title:: Treatment of volanesorsen in a patient with familial chylmicronaemia syndrome (FCS) due to homozygous c.337T>C(p.TRP113ARG) - mutation and impact of dietary incompliance: A case report
Authors:: De Gier, C.
Skacel, G.
Walleczek, N.-K.
Lischka, J.
Baumgartner, M.
Greber-Platzer, S.
Abstract:
Is Part Of:: Atherosclerosis. Volume 355(2022)
Journal:: Atherosclerosis
Issue:: Volume 355(2022)
Issue Display:: Volume 355, Issue 2022 (2022)
Year:: 2022
Volume:: 355
Issue:: 2022
Issue Sort Value:: 2022-0355-2022-0000
Page Start:: 65
Page End:
Publication Date:: 2022-08
Subjects:: Arteriosclerosis -- Periodicals
Electronic journals
616.136
Journal URLs:: http://www.sciencedirect.com/science/journal/00219150 ↗
http://www.clinicalkey.com/dura/browse/journalIssue/00219150 ↗
http://www.elsevier.com/journals ↗
DOI:: 10.1016/j.atherosclerosis.2022.06.421 ↗
Languages:: English
ISSNs:: 0021-9150
Deposit Type:: Legaldeposit
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗
Physical Locations:: British Library DSC - 1765.874000
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Ingest File:: 23301.xml