Establishing a Sickle Cell Disease Registry in Africa: Experience From the Sickle Pan-African Research Consortium, Kumasi-Ghana

Sickle cell disease (SCD) is the most common clinically significant hemoglobinopathy, characterized by painful episodes, anemia, high risk of infection, and other acute and chronic complications. In Africa, where the disease is most prevalent, large longitudinal data on patients and their outcomes a...

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Detalles Bibliográficos
Autores principales: Paintsil, Vivian, Amuzu, Evans Xorse, Nyanor, Isaac, Asafo-Adjei, Emmanuel, Mohammed, Abdul Razak, Yawnumah, Suraj Abubakar, Oppong-Mensah, Yaa Gyamfua, Nguah, Samuel Blay, Obeng, Paul, Dogbe, Elliot Eli, Jonas, Mario, Nembaware, Victoria, Mazandu, Gaston, Ohene-Frempong, Kwaku, Wonkam, Ambroise, Makani, Julie, Ansong, Daniel, Osei-Akoto, Alex
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8908904/
https://www.ncbi.nlm.nih.gov/pubmed/35281803
http://dx.doi.org/10.3389/fgene.2022.802355

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8908904/
https://www.ncbi.nlm.nih.gov/pubmed/35281803
http://dx.doi.org/10.3389/fgene.2022.802355

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