The genetic basis of asymptomatic codon 8 frame-shift (HBB:c25_26delAA) β(0) -thalassaemia homozygotes - Jiang, Zhihua; Luo, Hong-Yuan; Huang, Shengwen; Farrell, John J; Davis, Lance; Théberge, Roger; Benson, Katherine A; Riolueang, Suchada; Viprakasit, Vip; Al-Allawi, Nasir A S; Ünal, Sule; Gümrük, Fatma; et al. (British journal of haematology, 2016)
Keywords: beta-Thalassemia - genetics; Carrier Proteins - genetics; Diseases in Twins - genetics; Female; Fetal Hemoglobin - analysis; Fetal Hemoglobin - genetics; Frameshift Mutation; Genes, myb; Homozygote; Humans; Male; Middle Aged; Nuclear Proteins - genetics; Polymorphism, Single Nucleotide; Quantitative Trait Loci; Twins, Dizygotic - genetics; Young Adult; β0-Thalassaemia; HBS1L-MYB intergenic polymorphism; HbF quantitative trait loci; fetal haemoglobin; α-Thalassaemia