Population
15 probands from 11 families with primary lipoprotein lipase (LPL) deficiency
Design
Case_series
Authors
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Supports targeted LPL testing in suspected familial chylomicronemia; leaves open broader prevalence and diagnostic utility.
A specific genetic insertion accounts for a significant proportion of mutations causing primary lipoprotein lipase deficiency.
Langlois et al. (1989) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: