Cited by 61

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

Young, S G, Hubl, S T, Smith, R S, Snyder, S M, Terdiman, J F·1990·Journal of Clinical Investigation

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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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