טוען...
Loss of exon identity is a common mechanism of human inherited disease
It is widely accepted that at least 10% of all mutations causing human inherited disease disrupt splice-site consensus sequences. In contrast to splice-site mutations, the role of auxiliary cis-acting elements such as exonic splicing enhancers (ESE) and exonic splicing silencers (ESS) in human inher...
שמור ב:
| Main Authors: | , , , , |
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| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
Cold Spring Harbor Laboratory Press
2011
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3202274/ https://ncbi.nlm.nih.gov/pubmed/21750108 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1101/gr.118638.110 |
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