Rapid Screening of Multiple β-Globin Gene Mutations by RT-qPCR (CAT#: STEM-MT-0009-LGZ)

Introduction

Thalassemia is one of the most common hereditary diseases in the world. Blood routine and hemoglobin analysis are the main screening methods for thalassemia. Clinically, it is mainly divided into α-thalassemia and β-thalassemia, which is a hereditary hemolytic anemia caused by the deficiency or absence of synthesis of α or β globin chain due to the mutation or deletion of α or β globin gene, and the life span of red blood cells is shortened.