The DOI matches its Crossref record.
Familial hypobetalipoproteinemia caused by a mutation in the apolipoprotein B gene that results in a truncated species of apolipoprotein B (B-31). A unique mutation that helps to define the portion of the apolipoprotein B molecule required for the formation of buoyant, triglyceride-rich lipoproteins
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Genetic mutations in apo B100 are associated with altered VLDL secretion and plasma LDL levels.
“Accordingly, genetic mutations in apo B100 are associated with altered VLDL secretion and plasma LDL levels.4–6”
From (Pro)renin Receptor Inhibition Reprograms Hepatic Lipid Metabolism and Protects Mice From Diet-Induced Obesity and Hepatosteatosis (2018) · cites this paper as [6]
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Ren, L., Sun, Y., Lu, H., Ye, D., Han, L., Wang, N., Daugherty, A., Li, F., Wang, M., Su, F., et al. (2018) · Circulation Research · doi:10.1161/circresaha.117.312422 · Cited by 59
Metadata
- Authors
- Young, S. G., Hubl, S. T., Smith, R. S., Snyder, S. M., & Terdiman, J. F.
- Venue
- Journal of Clinical Investigation
- Published
- 1990-03-01
- Volume
- 85
- Issue
- 3
- Pages
- 933-942
- ISSN
- 0021-9738
- Cited by
- 61
- References
- 0
- Language
- en
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Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
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