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Hereditary cancer genes are highly susceptible to splicing mutations
Substitutions that disrupt pre-mRNA splicing are a common cause of genetic disease. On average, 13.4% of all hereditary disease alleles are classified as splicing mutations mapping to the canonical 5′ and 3′ splice sites. However, splicing mutations present in exons and deeper intronic positions are...
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| Vydáno v: | PLoS Genet |
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| Hlavní autoři: | , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Public Library of Science
2018
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5854443/ https://ncbi.nlm.nih.gov/pubmed/29505604 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pgen.1007231 |
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