α-Thalassaemia as a result of a novel splice donor site mutation of the α1 -globin gene
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1365-2141.2000.02225.x/fullpdf
Reference12 articles.
1. Nonsense mutations in the human β-globin gene affect mRNA metabolism;Baserga;Proceedings of the National Academy of Science of the United States of America,1988
2. α-Thalassaemia;Bernini;Baillieres Clinical Haematology,1998
3. An IVS I-117 (G→A) acceptor splice site mutation in the α1-globin gene is a nondeletional α-thalassaemia-2 determinant in an Indian population;Çürük;British Journal of Haematology,1993
4. Abnormal RNA splicing causes one form of α thalassaemia;Felber;Cell,1982
5. Phenotype variability of the dominant β-thalassaemia induced in four Dutch families by the rare cd121 (G→T) mutation;Giordano;Annals of Hematology,1998
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