Article
Molecular Characterization of β-Thalassemia Intermedia in Southeast Iran.
Hemoglobin - 1 Jun 2016
Miri-Moghaddam Ebrahim, Bahrami Sara, Naderi Majid, Bazi Ali, Karimipoor Morteza
Abstract excerpt
Inheritance of mild mutations within the β-globin gene and coinheritance of α-thalassemia (α-thal) are known as two important genetic modifiers in β-thalassemia (β-thal) intermedia (β-TI). We aimed to evaluate the spectrum of β- and α-thal mutations in β-TI patients in Southeast Iran. Common β- and α-globin gene mutations were detected by amplification refractory mutation system-polymerase chain reaction...
Topics
- DNA Mutational Analysis
- Female
- Gene Frequency
- Genotype
- Humans
- Iran
- Male
- Molecular Epidemiology
- Mutation
- Polymerase Chain Reaction
- alpha-Globins
- alpha-Thalassemia
