SINGLE NUCLEOTIDE POLYMORPHISMS ASSOCIATED WITH CARDIOVASCULAR DISEASE
摘要
<p>A method is provided for identifying a subject who has an increased risk for developing a cardiovascular disease. The method can include detecting an alteration in a portion of a LRP8 gene. The alternation can be located in at least one of exon 9, exon 17, exon 19, or intron 6 of the LRP8 gene. The presence of the alteration can be correlated with an increased risk for developing the cardiovascular disease.</p>
申请公布号
WO2008042762(A2)
申请公布日期
2008.04.10
申请号
WO2007US79862
申请日期
2007.09.28
申请人
THE CLEVELAND CLINIC FOUNDATION;WANG, QINY;TOPOL, ERIC, J.;SHEN, GONG-QING;LI, LIN;RAO, SHAOQI
