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Autor:
Hezekiah Isa, Emmanuel Okocha, Samuel Ademola Adegoke, Uche Nnebe-Agumadu, Aisha Kuliya-Gwarzo, Alayo Sopekan, Akinyemi Olugbenga Ofakunrin, Ngozi Ugwu, Abdul-Aziz Hassan, Chinatu Ohiaeri, Anazoeze Madu, Ijeoma Diaku-Akinwumi, Lilian Ekwem, Livingstone Gayus Dogara, Dorothy Okoh, James Jasini, Ahmed Girei, Timothy Ekwere, Angela Okolo, Umar Kangiwa, Juliet Lawson, Reuben Chianumba, Biobele Brown, Norah Akinola, Maxwell Nwegbu, Obiageli Nnodu
Publikováno v:
Frontiers in Genetics, Vol 14 (2023)
Background: Sickle cell disease (SCD) continues to pose physical and psychosocial burdens to patients, caregivers and health workers. Stakeholder engagement in the processes of policy making and implementation is increasingly becoming the cornerstone
Externí odkaz:
https://doaj.org/article/a8ddd0dd08ad491c80da2e340b2ef3de