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Autor:
Marcus Inyama Asuquo, Emmanuel Effa, Oluwabukola Gbotosho, Akaninyene Otu, Nicole Tofner, Ameh Soter, Bhayankaram Sruti-Prathivadhi, Noah Zetocha, Chisom Nwakama, William Ohobu Egbe, Jochen Guck, Andrew E. Ekpenyong
Sickle cell disorder (SCD) is a multisystem disease with heterogeneous phenotypes. Although all patients have the mutated haemoglobin (Hb) in the SS phenotype, the severity and frequency of complications are variable. When exposed to low oxygen tensi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::70bdc0777ed994004d4463769c7e1e41
https://doi.org/10.20944/preprints202202.0329.v1
https://doi.org/10.20944/preprints202202.0329.v1
