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Consent was provided by the patient to publish this clinical report.
Consent was provided from each participant for the results of this study to be published.
Consent was provided by the person responsible for 10 patients.
Informed consent was provided by each patient.
Written informed consent was provided by each donor.
Informed consent was provided by participants or, if the participant had died, from immediate family members.
Written informed consent was provided by all study participants.
Written informed consent was provided by all participants.
Written informed consent was provided by all patients.
Written informed consent was provided by all patients before study participation.
Written informed consent was provided by all study subjects.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com