A MUTATION IN THE POLYADENYLATION SIGNAL OF THE α2GLOBIN GENE (AATAA→AATA–) AS A CAUSE OF α THALASSAEMIA IN ASIAN INDIANS
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2141.1994.tb05008.x/fullpdf
Reference5 articles.
1. Hemoglobinopathies in India
2. A novel polyadenylation signal mutation in the α2-globin gene causing α thalassaemia
3. α-Thalassaemia caused by a polyadenylation signal mutation
4. Characterization of a new α° thalassaemia defect in the South African population
5. Hb H disease in a Turkish family resulting from the interaction of a deletional α-thalassaemia-1 and a newly discovered poly A mutation
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