The modifying effect of Xmn1-HBG2 on thalassemic phenotype is associated with its linked elements in the beta globin locus control region, including the palindromic site at 5'HS4. [electronic resource]
- Blood cells, molecules & diseases Jan 2012
- 1-5 p. digital
Publication Type: Journal Article
1096-0961
10.1016/j.bcmd.2011.10.001 doi
Adolescent Adult Alleles Case-Control Studies Child Chromatin--genetics Female Genes, Dominant Genetic Association Studies Genotype Heterozygote Homozygote Humans Inverted Repeat Sequences Iran Linkage Disequilibrium Locus Control Region--genetics Male Middle Aged Mutation Phenotype Polymorphism, Genetic beta-Globins--chemistry beta-Thalassemia--genetics