The use of base editing technology to characterize single nucleotide variants

Single nucleotide variants (SNVs) represent the most common type of polymorphism in the human genome. However, in many cases the phenotypic impacts of such variants are not well understood. Intriguingly, while some SNVs cause debilitating diseases, other variants in the same gene may have no, or lim...

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Detalles Bibliográficos
Autores principales: McDaniel, Sophia, Komor, Alexis, Goren, Alon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Research Network of Computational and Structural Biotechnology 2022
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9010703/
https://www.ncbi.nlm.nih.gov/pubmed/35465164
http://dx.doi.org/10.1016/j.csbj.2022.03.031

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9010703/
https://www.ncbi.nlm.nih.gov/pubmed/35465164
http://dx.doi.org/10.1016/j.csbj.2022.03.031

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