Identification and analysis of short indels inducing exon extension/shrinkage events
The search for genetic variants that act as causative factors in human diseases by disrupting the normal splicing process has primarily focused on single nucleotide variants (SNVs). It is worth noting that insertions or deletions (indels) have also been sporadically reported as causative disease var...
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| Principais autores: | , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Wiley
2024-10-01
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| coleção: | FEBS Open Bio |
| Assuntos: | |
| Acesso em linha: | https://doi.org/10.1002/2211-5463.13871 |
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