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Human SNPs resulting in premature stop codons and protein truncation
Single nucleotide polymorphisms (SNPs) constitute the most common type of genetic variation in humans. SNPs introducing premature termination codons (PTCs), herein called X-SNPs, can alter the stability and function of transcripts and proteins and thus are considered to be biologically important. In...
Tallennettuna:
| Päätekijät: | , , |
|---|---|
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
BioMed Central
2006
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3500177/ https://ncbi.nlm.nih.gov/pubmed/16595072 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1479-7364-2-5-274 |
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