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From association to causality: the new frontier for complex traits

Technological and analytical advances have led to an unprecedented catalog of genomic regions associated with a broad range of clinically relevant phenotypes in humans. However, some examples notwithstanding, the causes of the overwhelming majority of genetic diseases remain obscure. More importantl...

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Detalhes bibliográficos
Autor principal: Katsanis, Nicholas
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2009
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2664956/
https://ncbi.nlm.nih.gov/pubmed/19341494
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/gm23
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