Functional analysis of a beta-globin gene containing a TATA box mutation from a Kurdish Jew with beta thalassemia.
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry
Reference46 articles.
1. beta-Thalassemia in a Kurdish Jew. Single base changes in the T-A-T-A box.
2. The Thalassemia Syndromes;Weatherall,1981
3. Advances in thalassemia research
4. The Molecular Genetics of Human Hemoglobin
5. Nucleotide sequence analysis of the delta beta-globin gene region in humans.
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3. β-Thalassemia Intermedia with Exceptionally High Hemoglobin A2: Relationship to Mutations in the β-Gene Promoter;The American Journal of the Medical Sciences;1992-08
4. Organization of the gene for platelet glycoprotein IIb;Biochemistry;1990-02-06
5. Another Example of Japaneseβ-Thalassemia [-31 CAP (A→ G)];Hemoglobin;1989-01
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