Spectrum of Beta-Thalassemia Mutations in Potential Carriers with Microcytic Hypochromic Anemia from Mazandaran and Golestan, Northern Provinces of Iran

<div>List of mutations that the HbA2 level among heterozygous carrier individuals were normal (1 to 3.5%). Also, mean and standard deviations of cell blood count (CBC) index from these individuals are shown.</div>

BioMed Research International

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Table 4

Table 4: Spectrum of Beta-Thalassemia Mutations in Potential Carriers with Microcytic Hypochromic Anemia from Mazandaran and Golestan, Northern Provinces of Iran 

Table 4 | Spectrum of Beta-Thalassemia Mutations in Potential Carriers with Microcytic Hypochromic Anemia from Mazandaran and Golestan, Northern Provinces of Iran 