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See Latest ArticlesTIMP-2 Gene Polymorphism Is Associated with Intracerebral Hemorrhage
Cerebrovascular Diseases, 10/21/09
Reuter B et al. – The authors investigated a SNP 261 base pairs upstream of the start codon in exon 1 of TIMP–2. This data suggest that carriers of homozygosity for allele A are at increased risk of developing intracerebral hemorrhage.
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