Characterization and locus assignment of two α-globin variants present in the maltese population: Hb St. Luke's [α95(G2)Pro→Arg] and Hb Setif [α94(G1)Asp→Tyr]
Author:
Publisher
Informa UK Limited
Subject
Biochemistry (medical),Clinical Biochemistry,Genetics (clinical),Hematology
Link
http://www.tandfonline.com/doi/pdf/10.3109/03630269908996159
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1. Alpha-thalassemia caused by a large (62 kb) deletion upstream of the human alpha globin gene cluster
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4. Analysis of a 70 kb segment of DNA containing the human ζ and α-globin genes linked to their regulatory element (HS-40) in transgenic mice
5. A major positive regulatory region located far upstream of the human alpha-globin gene locus.
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1. Molecular diagnosis of α-thalassemia in a multiethnic population;European Journal of Haematology;2017-04-06
2. Molecular and hematological characteristics of a novel form of α-globin gene triplication: The hemoglobin St.Luke's-Thailand [α95(G2)Pro→Arg] or Hb St. Luke's [A2] HBA2;Clinical Biochemistry;2013-05
3. Detection of Hb Setif in North Iran and the Question of Its Origin: Iranian or Multiethnic?;Hemoglobin;2011-03-21
4. Hb Setif [α94(G1)Asp→Tyr (α2)] Detected in a Turkish Family;Hemoglobin;2003-01
5. Hb RAMPA [α95(G2)Pro→Ser (α2)] IN A FAMILY OF EUROPEAN ANCESTRY: DNA ANALYSIS CONFIRMS THECCG→TCG MUTATION AT CODON 95 OF THE α2-GLOBIN GENE; CLINICAL AND LABORATORY FEATURES;Hemoglobin;2002-01
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