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Pathogenicity and functional impact of non-frameshifting insertion/deletion variation in the human genome
Differentiation between phenotypically neutral and disease-causing genetic variation remains an open and relevant problem. Among different types of variation, non-frameshifting insertions and deletions (indels) represent an understudied group with widespread phenotypic consequences. To address this...
| Autores principales: | , , , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Public Library of Science
2019
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6594643/ https://www.ncbi.nlm.nih.gov/pubmed/31199787 http://dx.doi.org/10.1371/journal.pcbi.1007112 |