| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 8455781 | Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis | 2014 | 9 Pages |
Abstract
This data reveals that genetic variation in splicing-regulatory and particularly CpG sites might be related to disease predisposition and that in-silico analysis is useful for identifying sSNPs, which might be falsely identified as silent or synonymous.
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Authors
M. Karambataki, A. Malousi, S. Kouidou,