DOMINANT β THALASSAEMIA: MOLECULAR BASIS AND PATHOPHYSIOLOGY
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2141.1992.tb08132.x/fullpdf
Reference30 articles.
1. Hemoglobin Indianapolis (β112[G14] Arginine). An unstable β chain variant producing the phenotype of severe β-thalassemia;Adams;Journal of Clinical Investigation,1979
2. Isolation and characterization of the translation product of a β-globin gene nonsense mutation (β121 GAA â TAA);Adams;British Journal of Haematology,1990
3. Inclusion body β-thalassemia trait in a Swiss family is caused by an abnormal hemoglobin (Geneva) with an altered and extended β chain carboxy-terminus due to a modification in codon β114;Beris;Blood,1988
4. Hemoglobin Cranston, an unstable variant having an elongated β chain due to non-homologous crossover between two normal β chain genes;Bunn;Proceedings of the National Academy of Sciences of the United States of America,1975
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