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Published in 2019 at "Hemoglobin"
DOI: 10.1080/03630269.2019.1657886
Abstract: Abstract We identified a novel mutation of β-thalassemia (β-thal) in a heterozygous carrier from Azerbaijan. Phenotypical data and molecular mechanisms of codon 2 (–T) (HBB: c.9delT) was relevant to β0-thal. Additionally, we here report two…
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Keywords:
codon hbb;
hbb 9delt;
frameshift mutation;
novel frameshift ... See more keywords