Article
Silent β-thalassemia mutations at -101 (C>T) and -71 (C>T) and their coinheritance with the sickle cell mutation in Bahrain.
Hemoglobin - 1 Jan 2013
Al Moamen Nabeel J, Mahdi Fawzia, Salman Ebtihal, Ahmed Thabet, Abbas Ruqaya, Al Arrayed Shaikha, Sanad Hassan, Ahmed Al Alawi
Abstract excerpt
Silent β-thalassemia (β-thal) is a group of mutations affecting the β-globin gene that cannot be differentiated in heterozygote states from normal conditions by using conventional criteria for the diagnosis of β-thal trait. Here we report the existence of two silent β-thal mutations in the popula...
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