In the article by Henskens et al1, “Associations of the angiotensin II type 1 receptor A1166C and the endothelial NO synthase G894T gene polymorphisms with silent subcortical white matter lesions in essential hypertension,” which appeared in the September 2005 issue of Stroke, there was incorrect data presented in the results section of the abstract and in Table 3. The unstandardized β of the NOS3 T allele is 31.1 (CI, 3.6 to 58.4), not 3.1 (CI, 3.6 to 58.4) as given in the article.
The authors apologize for this error.
↵1[Correction for Vol 36, Number 9, September 2005. Pages 1869–1873.]