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Autor:
PO, Manafa, Okocha EC, O, Ekuma-Okereke, Aneke, JC, Ikegwuonu JA, NC, Ibe, Chukwuanukwu RC, Mbachu NA, KE, Nwene, Ebugosi RS, Manafa VI, Ihim AC
Background of study: Sickle Cell Disease (SCD) is an inherited haemoglobinopathy characterized by life-long haemolytic anaemia and vaso-occlussive crisis. Oxidative stress may be linked to its pathophysiology which may lead to several organ damage an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::288909c97e2cdee579e2b5ddff35d0ed
