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Functional SNP in an Sp1-binding site of AGTRL1 gene is associated with susceptibility to brain infarction.
A nonsynonymous SNP in PRKCH (protein kinase C eta) increases the risk of cerebral infarction.
SNPs on chromosome 5p15.3 associated with myocardial infarction in Japanese population.
Identification of 46 novel SNPs in the 130-kb region containing a myocardial infarction susceptibility gene on chromosomal band 6p21.
Identification of a novel non-coding RNA, MIAT, that confers risk of myocardial infarction.
Functional SNPs in the lymphotoxin-alpha gene that are associated with susceptibility to myocardial infarction.
A functional SNP in ITIH3 is associated with susceptibility to myocardial infarction.
SNPs in BRAP associated with risk of myocardial infarction in Asian populations.
A genome-wide association study identifies PLCL2 and AP3D1-DOT1L-SF3A2 as new susceptibility loci for myocardial infarction in Japanese.
Functional variation in LGALS2 confers risk of myocardial infarction and regulates lymphotoxin-alpha secretion in vitro.
A functional SNP in PSMA6 confers risk of myocardial infarction in the Japanese population.