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 ...
Please provide your email address to receive an email when new articles are posted on . Birth prevalence of sickle cell disease is one in 2,070 overall and one in 350 for non-Hispanic Black newborns.
Some results have been hidden because they may be inaccessible to you
Show inaccessible results
Feedback