Path to facilitate the prediction of functional amino acid substitutions in red blood cell disorders--a computational approach.
<h4>Background</h4>A major area of effort in current genomics is to distinguish mutations that are functionally neutral from those that contribute to disease. Single Nucleotide Polymorphisms (SNPs) are amino acid substitutions that currently account for approximately half of the known ge...
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| Autores principales: | , |
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| Formato: | article |
| Lenguaje: | EN |
| Publicado: |
Public Library of Science (PLoS)
2011
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| Acceso en línea: | https://doaj.org/article/16fff814cb374a7a997c0ed434ce85ee |
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