Rapid screening for glucose-6-phosphate dehydrogenase deficiency and haemoglobin polymorphisms in Africa by a simple high-throughput SSOP-ELISA method

BACKGROUND: Mutations in the haemoglobin beta-globin (HbB) and glucose-6-phosphate dehydrogenase (G6PD) genes cause widespread human genetic disorders such as sickle cell diseases and G6PD deficiency. In sub-Saharan Africa, a few predominant polymorphic variants of each gene account for a majority o...

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Detalles Bibliográficos
Autores principales: Enevold, Anders, Vestergaard, Lasse S, Lusingu, John, Drakeley, Chris J, Lemnge, Martha M, Theander, Thor G, Bygbjerg, Ib C, Alifrangis, Michael
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2005
Materias:
Methodology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1326224/
https://www.ncbi.nlm.nih.gov/pubmed/16356170
http://dx.doi.org/10.1186/1475-2875-4-61

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1326224/
https://www.ncbi.nlm.nih.gov/pubmed/16356170
http://dx.doi.org/10.1186/1475-2875-4-61

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