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Prior to interviews, formal introduction was given to patients regarding the purpose of seeking information and informed oral consent was obtained.
In addition, for specific events like pregnancy and its outcome, the informant was requested to give informed oral consent.
All participants were provided with information regarding the study, including the reasons for undertaking the research and provided informed oral consent.
All patients and control persons gave informed oral consent.
Participants provided separate informed oral consent for interviews, blood draws and blood storage.
An informed oral consent was obtained from the pregnant women and, in the case of the children, from the parents.
Inclusion criteria were age ≥ 18 years and informed oral consent.
Mandatory informed oral consent was obtained from all willing participants.
Study participants gave informed oral or written consent.
We obtained informed oral consent from all of the respondents.
An informed oral consent was obtained from children's parents/caregivers before enrolment.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com