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Disease Risk of Missense Mutations Using Structural Inference from Predicted Function

Advancements in sequencing techniques place personalized genomic medicine upon the horizon, bringing along the responsibility of clinicians to understand the likelihood for a mutation to cause disease, and of scientists to separate etiology from nonpathologic variability. Pathogenicity is discernabl...

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Detalhes bibliográficos
Main Authors: Horst, Jeremy A., Wang, Kai, Horst, Orapin V., Cunningham, Michael L., Samudrala, Ram
Formato: Artigo
Idioma:Inglês
Publicado em: 2010
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3095817/
https://ncbi.nlm.nih.gov/pubmed/20887259
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