INTERACTION OF THE α2 POLYADENYLATION SIGNAL MUTATION (AATAAA → AATA– –) AND α0-THALASSEMIA (– –SEA), RESULTING IN Hb H DISEASE IN A THAI PATIENT
Author:
Publisher
Informa UK Limited
Subject
Biochemistry, medical,Clinical Biochemistry,Genetics(clinical),Hematology
Link
http://www.tandfonline.com/doi/pdf/10.1081/HEM-100107875
Reference16 articles.
1. α-Thalassaemia caused by a polyadenylation signal mutation
2. The polyadenylation site mutation in the alpha-globin gene cluster
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