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Genetic basis of common human disease: Insight into the role of Missense SNPs from Genome Wide Association Studies
Recent genome wide association studies have led to the reliable identification of SNPs at a number of loci associated with increased risk of specific common human diseases. Each such locus implicates multiple possible candidate SNPs for involvement in disease mechanism. A variety of mechanisms may l...
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| Publicat a: | J Mol Biol |
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| Autors principals: | , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2015
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4893807/ https://ncbi.nlm.nih.gov/pubmed/25937569 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jmb.2015.04.014 |
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