Prediction of Deleterious Nonsynonymous Single-Nucleotide Polymorphism for Human Diseases

The identification of genetic variants that are responsible for human inherited diseases is a fundamental problem in human and medical genetics. As a typical type of genetic variation, nonsynonymous single-nucleotide polymorphisms (nsSNPs) occurring in protein coding regions may alter the encoded am...

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Detalles Bibliográficos
Autores principales: Wu, Jiaxin, Jiang, Rui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
Materias:
Review Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3572689/
https://www.ncbi.nlm.nih.gov/pubmed/23431257
http://dx.doi.org/10.1155/2013/675851

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3572689/
https://www.ncbi.nlm.nih.gov/pubmed/23431257
http://dx.doi.org/10.1155/2013/675851

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