Pioneering Informed Consent for Return of Research Results to Breast Cancer Patients Facing Barriers to Implementation of Genomic Medicine: The Kenyan BRCA1/2 Testing Experience Using Whole Exome Sequencing

INTRODUCTION: Obtaining informed consent from study participants and disseminating the findings responsibly is a key principle required for ethically conducted clinical and genetic research. Reports from African researchers providing feedback on insights gained during the return of whole exome seque...

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Detalhes bibliográficos
Publicado no:Front Genet
Main Authors: Torrorey-Sawe, Rispah, van der Merwe, Nicole, Mining, Simeon Kipkoech, Kotze, Maritha J.
Formato: Artigo
Idioma:Inglês
Publicado em: Frontiers Media S.A. 2020
Assuntos:
Genetics
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7089032/
https://ncbi.nlm.nih.gov/pubmed/32231682
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fgene.2020.00170
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