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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...
| Autores principales: | , , |
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| Formato: | Texto |
| Lenguaje: | English |
| Publicado: |
Public Library of Science
2008
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2423486/ https://www.ncbi.nlm.nih.gov/pubmed/18560565 http://dx.doi.org/10.1371/journal.pone.0002504 |