Molecular, haematological and clinical studies of a silent β-gene C → G mutation at 6 bp 3′ to the termination codon (+1480 C → G) in twelve Greek families-Reference-Cited by-同舟云学术

Molecular, haematological and clinical studies of a silent β-gene C → G mutation at 6 bp 3′ to the termination codon (+1480 C → G) in twelve Greek families

Published:1998-10 Issue:1 Volume:103 Page:45-51
ISSN:0007-1048
Container-title:British Journal of Haematology
language:en
Short-container-title:British Journal of Haematology

Author:

Maragoudaki ,Vrettou ,Kanavakis ,Traeger-Synodinos ,Metaxotou-Mavrommati ,Kattamis

Publisher

Wiley

Subject

Hematology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1365-2141.1998.00966.x/fullpdf

Reference32 articles.

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2. A novel 13 bp deletion in the 3′ UTR of the β globin gene causes β thalassemia in a Turkish patient;Basak;Hemoglobin,1993

3. Two novel β thalassemia mutations in the 5′ and 3′ noncoding regions of the β globin gene;Cai;Blood,1992

4. Clegg , J.B. 1983 Methods in Haematology: the Thalassaemias 54 73

5. The relative levels of βA and βS mRNAs in HbS heterozygotes and in patients with HbS-β+ thalassaemia or HbS-β+ HPFH combinations;Dimovsky;British Journal of Haematology,1994

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