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Prediction of phenotypes of missense mutations in human proteins from biological assemblies

Single nucleotide polymorphism (SNPs) are the most frequent variation in the human genome. Non-synonymous SNPs that lead to missense mutations can be neutral or deleterious, and several computational methods have been presented that predict the phenotype of human missense mutations. These methods em...

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Detalhes bibliográficos
Main Authors: Wei, Qiong, Xu, Qifang, Dunbrack, Roland L.
Formato: Artigo
Idioma:Inglês
Publicado em: 2012
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3552143/
https://ncbi.nlm.nih.gov/pubmed/22965855
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/prot.24176
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