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Clinical Application

Beta-mediterranean anemia (β-thalassemia) is a kind of monogenic inheritance hemopathy due to expression imbalance of peptide chain caused by β-globin gene mutation. It is mostly caused by β-globin gene mutation. The commonly seen mutation sites are CD41/42, IVS-Ⅱ-654, -28, CD71/72, etc.

Intended Use

General Specification

Packing Specifications

Demonstration of Results