Two novel polyadenylation mutations leading to β+-thalassaemia
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2141.1990.00122.x/fullpdf
Reference16 articles.
1. β -Thalassemia in American Blacks: Novel mutations in the ‘TATA’ box and an acceptor splice site;Antonarakis;Proceedings of the National Academy of Sciences of the United States of America,1984
2. High-performance liquid chromatographic separation of human haemoglobins. Simultaneous quantitation of foetal and glycated haemoglobins;Bisse;Journal of Chromatography,1988
3. The molecular basis of β-thalassemia in Lebanon: Application to prenatal diagnosis;Chehab;Blood,1987
4. Clinical and genetic heterogeneity in Black patients with homozygous β-thalassemia from the southeastern United States;Gonzalez-Redondo;Blood,1988
5. Characterization of three types of βthalassemia resulting from a partial deletion of the β-globin gene;Gonzalez-Redondo;Hemoglobin,1989
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1. 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
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