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Influence of common and rare genetic variation on warfarin dose among African–Americans and European–Americans using the exome array
AIM: We conducted a genome-wide association study using the Illumina Exome Array to identify coding SNPs that may explain additional warfarin dose variability. PATIENTS & METHODS: Analysis was performed after adjustment for clinical variables and genetic factors known to influence warfarin dose...
Gorde:
| Argitaratua izan da: | Pharmacogenomics |
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| Egile Nagusiak: | , , , , , , , , , |
| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
Future Medicine Ltd
2017
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| Gaiak: | |
| Sarrera elektronikoa: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5619051/ https://ncbi.nlm.nih.gov/pubmed/28686080 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2217/pgs-2017-0046 |
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