| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 11030650 | Atherosclerosis | 2018 | 6 Pages |
Abstract
Our data indicate that in addition to variants in LDLR, APOB, PCSK9, APOE, LDLRAP1, and STAP1, variants in ABCG5/8, CYP27A1, LIPA, LIPC, and LIPG may be associated with hypercholesterolemia and such information should be used to optimize therapy.
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Authors
Pablo Corral, Andrew S. Geller, Eliana Y. Polisecki, Graciela I. Lopez, Virginia G. Bañares, Leonardo Cacciagiu, Gabriela Berg, Robert A. Hegele, Ernst J. Schaefer, Laura E. Schreier,