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pro vyhledávání: '"William Egbe"'
Autor:
Marcus Inyama Asuquo, Emmanuel Effa, Oluwabukola Gbotosho, Akaninyene Otu, Nicole Toepfner, Soter Ameh, Sruti-Prathivadhi Bhayankaram, Noah Zetocha, Chisom Nwakama, William Egbe, Jochen Guck, Andrew Ekpenyong
Publikováno v:
Applied Sciences, Vol 12, Iss 9, p 4394 (2022)
Sickle cell disorder (SCD) is a multisystem disease with heterogeneous phenotypes. Although all patients have the mutated hemoglobin (Hb) in the SS phenotype, the severity and frequency of complications are variable. When exposed to low oxygen tensio
Externí odkaz:
https://doaj.org/article/09c8d48495fd41ad8d4a84156d0b538d
