Article
Occurrence of the Codon 24 (A > T) Mutation in the Mauritanian Population.
Hemoglobin - 1 Jan 2015
Veten Fatimetou, Ghaber Sidi, Habti Nordine, Houmeida Ahmed
Abstract excerpt
Using direct DNA sequencing, we identified the codon 24 (A > T) (HBB: c.72T > A, p.Gly24Gly), mutation in two out of 15 Mauritanian β-thalassemia (β-thal) carriers. Both were of Black origin and had hematological indices compatible with mild β-thal minor. Could this variant be more common than expected in the Black Mauritanian population?
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