Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1968130 | Clinica Chimica Acta | 2006 | 6 Pages |
Abstract
The heterozygous carriers of 2 different mutations in the LPL gene had different VLDL apo B FCR, and from normal to slightly low HDL apolipoprotein FCR and PR. These results disagree with the putative enhanced apo AI FCR in LPL deficient patients and suggest the need to reconsider the effects of LPL activity on HDL metabolism.
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Authors
Oscar Pérez-Méndez, Nathalie Duhal, Brigitte Lacroix, Jean-Paul Bonte, Jean-Charles Fruchart, Gérald Luc,