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A prospective replication study of five gene variants previously associated with risk of myocardial infarction

✍ Scribed by R. Y. L. ZEE; S. E. MICHAUD; H. H. HEGENER; K. A. DIEHL; P. M. RIDKER


Book ID
109151681
Publisher
John Wiley and Sons
Year
2006
Tongue
English
Weight
480 KB
Volume
4
Category
Article
ISSN
1538-7933

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The Werner syndrome (WS) is a rare autosomal recessive progeroid syndrome characterized by the premature onset of multiple age-related disorders, including atherosclerosis, cancer, non-insulin-dependent diabetes mellitus (NIDDM), ocular cataracts and osteoporosis [Epstein et al., 1966]. The major ca