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Article

Low rate of production of apolipoproteins B100 and AI in 2 patients with Anderson disease (chylomicron retention disease).

Arteriosclerosis, thrombosis, and vascular biology - 1 Jun 2012

Ouguerram Khadija, Zaïr Yassine, Kasbi-Chadli Fatima, Nazih Hassane, Bligny Dominique, Schmitz Jacques, Aparicio Thomas, Chétiveaux Maud, Magot Thierry, Aggerbeck Laurence P, Samson-Bouma Marie Elisabeth, Krempf Michel

Abstract excerpt

OBJECTIVE: Anderson disease is a rare inherited lipid malabsorption syndrome associated with hypocholesterolemia and linked to SAR1B mutations. The aim of this article was to analyze the mechanisms responsible for the low plasma apolipoprotein Apo-B100 and Apo-AI in 2 patients with Anderson disease. METHODS AND RESULTS: A primed constant infusion of (13)C-leucine was administered for 14 hours to determine the...

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Identifiers

PMID: 22441101
DOI: 10.1161/ATVBAHA.112.245076

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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