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Lack of Association of the 3′-UTR Polymorphism (rs1017) in theISL1Gene and Risk of Congenital Heart Disease in the White Population

✍ Scribed by Monica Cresci, Cecilia Vecoli, Ilenia Foffa, Silvia Pulignani…

Book ID: 120763970
Publisher: Springer
Year: 2012
Tongue: English
Weight: 199 KB
Volume: 34
Category: Article
ISSN: 0172-0643
DOI: 10.1007/s00246-012-0578-z

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## 817 ated with increased risk for AD, at least in the Korean population. Nevertheless, it cannot be excluded that the association between IL-1A (-889) C/T polymorphism and AD observed in previous studies might be the result of linkage disequilibrium with a yet unidentified gene on chromosome 2.