Open AccessGenetic Etiology of Isolated Low HDL Syndrome
Author(s) -
Robert S. Kiss,
Nihan Kavaslar,
Keiichiro Okuhira,
Mason W. Freeman,
Stephanie Wälter,
Ross W. Milne,
Ruth McPherson,
Yves L. Marcel
Publication year - 2007
Publication title -
arteriosclerosis thrombosis and vascular biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.007
H-Index - 270
eISSN - 1524-4636
pISSN - 1079-5642
DOI - 10.1161/atvbaha.106.137646
Subject(s) - abca1 , efflux , tangier disease , reverse cholesterol transport , cholesterol , biology , genetics , cholesterylester transfer protein , phenotype , apolipoprotein b , endocrinology , lipoprotein , medicine , gene , transporter
We have used a multitiered approach to identify genetic and cellular contributors to high-density lipoprotein (HDL) deficiency in 124 human subjects.
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