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Identification of Novel Hb Guiyang [HBA2: c.151C > A α2 50 (CE8) His- Asn] and Phenotype- Genotype Correlation of ...
Introduction Hemoglobinopathy is a type of autosomal monogenic genetic disease with a globin gene mutation that results in insufficient hemoglobin synthesis or structural abnormalities, which is widely distributed worldwide, especially in the Mediterranean …