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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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| Asıl Yazarlar: | , , |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
2011
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| Konular: | |
| Online Erişim: | 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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