HEMOGLOBIN H DISEASE, NONDELETIONAL
National Institutes of Health
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Abstract About 10.0% of α-thalassemia (α-thal) cases are due to point mutations, small deletions, or insertions of one or more…
Because of the life‐consuming treatment and severe consequences associated with thalassemia, it is more effective to prevent than…
A rare nondeletional α-thalassemia-2 (α-thal-2) allele was identified in a Thai boy with Hb H (β4) disease. The proband has…
The interaction of the nondeletional α-thalassemia (α-thal) mutations with the Southeast Asian double α-globin gene deletion…