Cargando…
How should we address the inevitable harms from non‐negligent variant reclassification in predictive genetic testing?
The process of interpreting genetic variants, in which experts use all available evidence to determine whether an identified variant is associated with a current or future disease, is both scientific and nevertheless subjective. In this paper, we summarize the existing evidence that any given varian...
| Autores principales: | , , , , , , |
|---|---|
| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
John Wiley and Sons Inc.
2022
|
| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10092710/ https://www.ncbi.nlm.nih.gov/pubmed/36260514 http://dx.doi.org/10.1002/jgc4.1638 |