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Genome-wide identification of exon extension/shrinkage events induced by splice-site-creating mutations
Mutations that affect phenotypes have been identified primarily as those that directly alter amino acid sequences or disrupt splice sites. However, some mutations not located in functionally important sites can also affect phenotypes, such as splice-site-creating mutations (SCMs). To investigate how...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Taylor & Francis
2022
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9639565/ https://www.ncbi.nlm.nih.gov/pubmed/36329613 http://dx.doi.org/10.1080/15476286.2022.2139111 |