β-thalassemia intermedia due to compound heterozygosity for two β-globin gene promoter mutations, including a novel TATA box deletion
Author:
Publisher
Wiley
Subject
Oncology,Hematology,Pediatrics, Perinatology and Child Health
Reference14 articles.
1. β-Thalassemia
2. Frequencies of thalassemia in American blacks
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4. Phenotype—genotype relationships in monogenic disease: lessons from the thalassaemias
5. DNA sequence variation associated with elevated fetal G gamma globin production
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1. Novel Promoter Mutation (HBB:C.-139_-138del) Associated with β-Thalassemia Trait Detected by Next-Generation Sequencing in Southern China;Hemoglobin;2023-01-02
2. Two Novel and Five Rare Mutations in the Non Coding Regions of the β-Globin Gene in the Iranian Population;Hemoglobin;2020-07-03
3. Thalassemias;Rodak's Hematology;2020
4. Phenotypic evaluations of −223 T>C (HBB:c.−223T>C) nucleotide substitution in the promoter region of β-globin gene;Blood Cells, Molecules, and Diseases;2015-10
5. Two new β+-thalassemia mutation [β -56 (G → C); HBBc. −106 G → C] and [β −83 (G → A); HBBc. −133 G → A] described among the Tunisian population;American Journal of Human Biology;2015-03-07
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