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Hypobetalipoproteinemia, Familial, Apolipoprotein B

"Hypobetalipoproteinemia, Familial, Apolipoprotein B" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure, which enables searching at various levels of specificity.

An autosomal dominant disorder of lipid metabolism. It is caused by mutations of APOLIPOPROTEINS B, main components of CHYLOMICRONS and BETA-LIPOPROTEINS (low density lipoproteins or LDL). Features include abnormally low LDL, normal triglyceride level, and dietary fat malabsorption.

This graph shows the total number of publications written about "Hypobetalipoproteinemia, Familial, Apolipoprotein B" by people in Harvard Catalyst Profiles by year, and whether "Hypobetalipoproteinemia, Familial, Apolipoprotein B" was a major or minor topic of these publication.
Bar chart showing 2 publications over 2 distinct years, with a maximum of 1 publications in 2014 and 2019
To see the data from this visualization as text, click here.
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Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.