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All project staff completed Protection of Human Research Subjects training prior to beginning the study, and clinical samples were collected after written or verbal informed consent was obtained from participants. For adult participants, written consent was obtained from literate patients, and oral consent documented by a thumb print was obtained from illiterate patients (approved by the ethical committees). For child participants, assent was obtained from the participant, in addition to written or oral consent from their parent or legal guardian.","order":1,"name":"Ethics","group":{"name":"EthicsHeading","label":"Ethics approval and consent to participate"}},{"value":"Not Applicable.","order":2,"name":"Ethics","group":{"name":"EthicsHeading","label":"Consent for publication"}},{"value":"The authors declare that they have no competing interests.","order":3,"name":"Ethics","group":{"name":"EthicsHeading","label":"Competing interests"}}],"article-number":"572"}}