| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 9956889 | International Journal of Cardiology | 2005 | 5 Pages |
Abstract
Carriers for the ABCC6 R1141X mutation, which is frequent and confers a high risk of premature coronary artery disease, do not commonly have skin or eye abnormalities consistent with a mild PXE phenotype.
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Authors
Jurgen J. Wegman, Xiaofeng Hu, Hendra Tan, Arthur A.B. Bergen, Mieke D. Trip, John J.P. Kastelein, Yvo M. Smulders,