Analysis of α-hemoglobin-stabilizing protein (AHSP) gene as a genetic modifier to the phenotype of β-thalassemia in Southern China
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Hematology,Molecular Biology,Molecular Medicine
Reference20 articles.
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2. The Thalassemia Syndromes;Weathedrall,2001
3. A Czechoslovakian teenager with Hb E-beta zero-thalassemia [IVS-I-1 (G—A)] complicated by the presence of an alpha-globin gene triplication;Indrak;Ann. Hematol.,1991
4. Phenotype–genotype relationships in monogenic disease: lessons from the thalassaemias;Weatherall;Nat. Rev. Genet.,2001
5. An abundant erythroid protein that stabilizes free alpha hemoglobin;Kihm;Nature,2002
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1. Impact of α-Globin Gene Expression and α-Globin Modifiers on the Phenotype of β-Thalassemia and Other Hemoglobinopathies: Implications for Patient Management;International Journal of Molecular Sciences;2024-03-17
2. The Potential of ANK1 to Predict Parkinson’s Disease;Genes;2023-01-15
3. Alpha-hemoglobin-stabilizing protein (AHSP): a modulatory factor in β-thalassemia;International Journal of Hematology;2020-01-01
4. Association of alpha hemoglobin–stabilizing protein (AHSP) gene mutation and disease severity among HbE—beta thalassemia patients;Annals of Hematology;2019-06-13
5. A molecular study on the role of alpha-hemoglobin-stabilizing protein in hemoglobin H disease;Annals of Hematology;2017-03-23
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