Segmental duplications involving the α-globin gene cluster are causing β-thalassemia intermedia phenotypes in β-thalassemia heterozygous patients
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Hematology,Molecular Biology,Molecular Medicine
Reference29 articles.
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4. A case of non-β-globin gene linked β-thalassaemia in a Dutch family with two additionaland α-gene defects: the common -α3.7 deletion and the rare IVS-I-116 (A→G) acceptor splice site mutation;Giordano;Br. J. Haematol.,1998
5. The haematological effects of glucose-6-phosphate dehydrogenase deficiency and thalassaemia trait: interaction between the two genes at the phenotype level;Piomelli;Br. J. Haematol.,1969
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