IS IT DOMINANTLY INHERITED β THALASSAEMIA OR JUST A β-CHAIN VARIANT THAT IS HIGHLY UNSTABLE?
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1365-2141.1999.01492.x/fullpdf
Reference51 articles.
1. Hemoglobin Indianapolis (beta 112[G14] arginine). An unstable beta-chain variant producing the phenotype of severe beta-thalassemia.
2. Isolation and characterization of the translation product of a β-globin gene nonsense mutation (β121 GAA→TAA)
3. The dominant β‐thalassaemia in a Spanish family is due to a frameshift that introduces an extra CGG codon (=arginine) at the 5′ end of the second exon
4. A Case of Hemoglobin Indianapolis [β112(G14) Cys→Arg] in an Individual from Cordoba, Spain
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