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Copy Number Variants in pharmacogenetic genes
Variation in drug efficacy and toxicity remains an important clinical concern. Presently, single nucleotide polymorphisms (SNP) only explain a portion of this problem, even in situations where the pharmacological trait is clearly heritable. The Human CNV Project identified copy number variations (CN...
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| Autors principals: | , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2011
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3092840/ https://ncbi.nlm.nih.gov/pubmed/21388883 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.molmed.2011.01.007 |
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