Article
The spectrum of β-thalassemia mutations in Kermanshah Province in West Iran and its association with hematological parameters.
Hemoglobin - 1 Jan 2013
Mehrabi Masomeh, Alibakhshi Reza, Fathollahi Soheila, Farshchi Mohammad Reza
Abstract excerpt
β-Thalassemia (β-thal) is a hereditary autosomal disorder with decreased or absent β-globin chain synthesis. Two hundred and one unrelated β-thal carriers, attending the Kermanshah Medical Genetics Laboratory, Kermanshah, Iran, were investigated for β-globin gene mutations by amplification refrac...
Topics
- Erythrocyte Indices
- Geography
- Humans
- Iran
- Mutation
- Phenotype
- beta-Globins
- beta-Thalassemia