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Cataloging Coding Sequence Variations in Human Genome Databases
BACKGROUND: With the recent growth of information on sequence variations in the human genome, predictions regarding the functional effects and relevance to disease phenotypes of coding sequence variations are becoming increasingly important. The aims of this study were to catalog protein-coding sequ...
Tallennettuna:
| Päätekijät: | , , , |
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| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Public Library of Science
2008
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2570488/ https://ncbi.nlm.nih.gov/pubmed/18974781 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0003575 |
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