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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...

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Shranjeno v:
Bibliografske podrobnosti
izdano v:J Community Genet
Main Authors: Makhnoon, Sukh, Garrett, Lauren Thomas, Burke, Wylie, Bowen, Deborah J., Shirts, Brian H.
Format: Artigo
Jezik:Inglês
Izdano: Springer Berlin Heidelberg 2018
Teme:
Online dostop: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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