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Key terms:
thalassemia
chains
disease
hemoglobin
genetic
blood
prevalence
cell
mediterranean
affected
beta
autosomal
populations
recessive
carrier
patients
anemia
globin chains
chromosome
produces
screening
inherited
thalassemia major
treatment
concentrations
reduced
abnormal
mutations
encoded
disorders
beta thalassemia
transplantation
excess
delta
genetic counseling
trait
loci
iron chelation
cyprus
thalassa
hemoglobin c
synthesis
malaria
therapy
alpha
protection against
greece
globin proteins
severe
formation
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