A Novel β-Thalassemic Allele Due to a Two Nucleotide Deletion: β76 (−GC)
Author:
Publisher
Informa UK Limited
Subject
Biochemistry, medical,Clinical Biochemistry,Genetics(clinical),Hematology
Link
http://www.tandfonline.com/doi/pdf/10.1080/03630260601057021
Reference12 articles.
1. The Thalassaemia Syndromes
2. Occurrence of hereditary spherocytosis and β thalassaemia in the same family: globin chain synthesis and visco diffractometric studies
3. Rapid analysis of -α3.7thalassaemia and αααanti 3.7triplication by enzymatic amplification analysis
4. Rapid detection of α-thalassaemia deletions and α-globin gene triplication by multiplex polymerase chain reactions
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1. A New Intergenicα-Globin Deletion (α–αΔ125) Found in a Kabyle Population;Hemoglobin;2016-02-25
2. Compound heterozygote condition in beta thalassemia major due to a novel single nucleotide deletion (-T) at codon 69 in association with IVS 1-5 (G>C) mutation;International Journal of Laboratory Hematology;2012-03-12
3. Elevated Hemoglobin A2 as a Marker for .BETA.-Thalassemia Trait in Pregnant Women;The Tohoku Journal of Experimental Medicine;2011
4. First Identification of a Point Mutation at Position −83 (G>A) of the β-Globin Gene Promoter;Hemoglobin;2009-01
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