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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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Main Authors: | , , |
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Formato: | Artigo |
Idioma: | Inglês |
Publicado em: |
2012
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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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