Supplemental material
AJOB Empirical Bioethics
Volume 11, 2020 - Issue 4
Articles
The Meaning of Informed Consent: Genome Editing Clinical Trials for Sickle Cell Disease
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Brittany M. Hollistera Social and Behavioral Research Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, USAhttps://orcid.org/0000-0001-9913-4663View further author information
https://orcid.org/0000-0001-9913-4663View further author information, , , Sara Chandros Hullb Department of Bioethics, Clinical Center, National Institutes of Health, Bethesda, Maryland, USA;c Bioethics Core, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, USAhttps://orcid.org/0000-0001-8742-4997View further author information
https://orcid.org/0000-0001-8742-4997View further author information & Vence L. Bonhama Social and Behavioral Research Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, USACorrespondence[email protected]
https://orcid.org/0000-0002-3649-5442View further author information
https://orcid.org/0000-0002-3649-5442View further author information