Article
Spectrum of Beta-Thalassemia Mutations in Potential Carriers with Microcytic Hypochromic Anemia from Mazandaran and Golestan, Northern Provinces of Iran.
BioMed research international - 1 Jan 2024
Mousavi Seyed Saeed, Karami Hossein, Tamadoni Ahmad, Mahmoudi Hassan, Shekarriz Ramin, Siami Rita, Hashemi-Soteh Mohammad Bagher
Abstract excerpt
Introduction: β-Thalassaemia is the most common genetic disorder and is considered as a major public health concern in Iran. Different countrywide studies have shown a heterogeneous mutational basis of β-thalassaemia with different frequencies in each area. This study is aimed at investigating the common and rare mutations in Mazandaran and Golestan, northern provinces of Iran. Methods: 5425 microcytic and...
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