Structure and expression of a cloned β o thalassaemic globin gene.
We have cloned the single beta-globin gene from an Italian patient who is a double heterozygote for beta o/delta beta o thalassaemia. RNA isolated from nucleated red cells from this patient can be translated in vitro to give detectable levels of A gamma-
Flavell, R.A. (Richard) +6 more
core
Abnormally Low Hemoglobin A1c Due to a Heterozygous Alpha-Globin Variant (Hb I; HBA2 c.49A>G, p.Lys17Glu) in a Geriatric Patient. [PDF]
Moshiri KA, Mahmodian M.
europepmc +1 more source
Diagnostic Challenges of Hemoglobin (Hb) Hekinan with deletional α<sup>0</sup>-thalassemia and β<sup>0</sup>-thalassemia During Prenatal Screening for Fetal Hb E/β-Thalassemia Risk. [PDF]
Chumnumsiriwath P +7 more
europepmc +1 more source
Different genes in the beta-like globin locus are expressed at specific times during development, This is controlled, in part, by competition between the genes for activation by the locus control region, In mice, gene inactivation of the erythroid ...
Perkins, AC +4 more
core
Mapping long-read sequences to a complete reference genome reveals uncaptured variants across the β-Globin cluster in Africans with sickle cell disease. [PDF]
Lurie P +24 more
europepmc +1 more source
Longstanding Microcytosis with a Thalassaemia-Like Phenotype and Inconclusive Molecular Testing: A Case Report. [PDF]
Kuriri FA.
europepmc +1 more source
Genetic profiles and hematological characteristics of the α-Hb variant Hb Chumphae (HBA2:c.32T>A) in association with -<sup>SEA</sup> deletion α<sup>0</sup>-thalassemia. [PDF]
Sihathip P +5 more
europepmc +1 more source
Arterial iron regulates vasodilation during anemia via endothelial holo-α-globin.
Dunaway LS +14 more
europepmc +1 more source

