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The ‘Common Disease-Common Variant’ Hypothesis and Familial Risks
The recent large genotyping studies have identified a new repertoire of disease susceptibility loci of unknown function, characterized by high allele frequencies and low relative risks, lending support to the common disease-common variant (CDCV) hypothesis. The variants explain a much larger proport...
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| Autori principali: | , , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Public Library of Science
2008
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2423486/ https://ncbi.nlm.nih.gov/pubmed/18560565 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0002504 |
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