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A genome-wide association study of venous thromboembolism identifies risk variants in chromosomes 1q24.2 and 9q
OBJECTIVES: To identify venous thromboembolism (VTE) disease-susceptibility genes. PATIENTS/METHODS: We performed in silico genome wide association (GWAS) analyses using genotype data imputed to ~2.5 million single nucleotide polymorphisms (SNPs) from adults with objectively-diagnosed VTE (n=1503),...
Tallennettuna:
| Päätekijät: | , , , , , , |
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| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
2012
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3419811/ https://ncbi.nlm.nih.gov/pubmed/22672568 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1538-7836.2012.04810.x |
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