Population
Patients with familial combined hyperlipidemia (FCHL)
Design
Review
Authors
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Supports FCHL genetic heterogeneity; leaves open full locus identification and clinical translation.
Familial combined hyperlipidemia is a genetically heterogeneous disorder involving multiple modifier and major genes.
Aouizerat et al. (1999) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: