It is known that heterozygous mutations in the HBB gene, which encodes β-globin, are the cause of inherited β-thalassemia. A new case report describes a novel frameshift mutation in the HBB gene ...
HBB-β S: An A greater than T point mutation results in the substitution of glutamate for valine in the sixth amino acid position (or seventh, if the… Development of SCD depends on whether the ...
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