Population
2 patients homozygous for familial hyperbetalipoproteinaemia
Design
Case_series
Authors
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Does not inform clinical management; leaves open the functional role of this anomalous LDL.
Patients homozygous for familial hyperbetalipoproteinaemia possess an anomalous LDL particle characterized by altered triglyceride and cholesterol proportions but otherwise normal structural properties.
Mills et al. (1976) studied this question.
Synapse has enriched 3 closely related papers on similar clinical questions. Consider them for comparative context: