A Novel 13 BP Deletion in the 3′UTR of the β-Globin Gene Causes β-Thalassemia in a Turkish Patient
Author:
Publisher
Informa UK Limited
Subject
Biochemistry (medical),Clinical Biochemistry,Genetics (clinical),Hematology
Link
http://www.tandfonline.com/doi/pdf/10.3109/03630269309043496
Reference17 articles.
1. The molecular basis of β-thalassemia in Turkey
2. Generation of single-stranded DNA by the polymerase chain reaction and its application to direct sequencing of the HLA-DQA locus.
3. Clinical and genetic heterogeneity in black patients with homozygous beta-thalassemia from the southeastern United States
4. Severe Hb S-β°-thalassaemia with a T → C substitution in the donor splice site of the first intron of the β-globin gene
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1. Evaluation of the Function of a Rare Variant in the 3'-Untranslated Region of the β-Globin Gene;Hemoglobin;2022-11-02
2. Compound heterozygosity of a silent beta‐thalassemia mutation at the 3′‐untranslated region ( HBB : c.*132 C>T) and beta‐zero thalassemia results in thalassemia intermedia;Pediatric Blood & Cancer;2020-01-13
3. Population-Based Genetic Study of β-Thalassemia Mutations in Mardan Division, Khyber Pakhtunkhwa Province, Pakistan;Hemoglobin;2017-03-04
4. Premarital Genetic Diagnosis Revealed Co-heredity Nature of Beta Globin Gene 25-26 del AA and 3’UTR+101 G-C Variants in Two Beta Thalassemia Heterozygotes;Turkish Journal of Hematology;2017-03-01
5. Co-heredity of silent CAP + 1570 T>C (HBB:c*96T>C) defect and severe β-thal mutation: a cause of mild β-thalassemia intermedia;International Journal of Laboratory Hematology;2015-09-29
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