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Experiences of patients seeking to participate in variant of uncertain significance reclassification research
Patients’ understanding of a genetic variant of unknown clinical significance (VUS) is likely to influence beliefs about risk implications, consequent medical decisions, and other actions such as involvement in research. We interviewed 26 self-selected participants with a clinically identified VUS b...
Gardado en:
| Publicado en: | J Community Genet |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Springer Berlin Heidelberg
2018
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6435771/ https://ncbi.nlm.nih.gov/pubmed/30027524 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s12687-018-0375-3 |
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