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...

Descripción completa

Detalles Bibliográficos
Autores principales: Hemminki, Kari, Försti, Asta, Bermejo, Justo Lorenzo
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2008
Materias:
Research Article
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

Internet

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

Ejemplares similares