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Introduction
β‐thalassemia is a severe hereditary hemolytic anemia. Due to the diversity of mutations spectrum, β‐thalassemia manifests a highly heterogeneous clinical severity. We noted that a previous report characterized HBB:c.313delA, at the end of exon 2, as a β‐thalassemia trait rather than dominant β‐thalassemia, the classification given to similar mutations. We further explored the impact...
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