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Informed subject consent was obtained before any measurements were taken.
Informed subject consent was provided with completion of the baseline interview, and Institutional Review at the National University of Singapore, University of Pittsburgh, and the University of Minnesota granted approval of this study.
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All subjects provided informed consent and consent for publication.
Details on IRB review, informed consent, subject exclusion criteria, the sampling protocols, and timeline can be found in previous publications1,13,40.
After complete description of the study to the subjects, informed written consent was obtained.
All subjects gave informed consent and signed approved consent forms.
After being approached and providing informed written consent, subjects had clinical and laboratory data collected.
Each subject gave informed written consent to the study.
The approved protocol and subject informed consent states that data will only be accessible to the study team.
All study subjects provided informed written consent.
All subjects gave informed written consent before the study.
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