Severity of β-thalassemia due to genotypes involving the IVS-I-6 (T→C) mutation
Author:
Publisher
Wiley
Subject
Hematology
Reference30 articles.
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1. A Novel β-Thalassemia Mutation [IVS-I-6 (T>G), HBB: c.92+6T>G] in a Chinese Family;Hemoglobin;2020-01-02
2. Presence of the IVS-I-6-Mutated Allele in Beta-Thalassemia Major Patients Correlates with Extramedullary Hematopoiesis Incidence;Acta Haematologica;2017
3. First Detection of a Splice Siteβ-Thalassemia Mutation, IVS-I-6 (T > C) (HBB: c.92 + 6T > C) in a Chinese Family;Hemoglobin;2015-04-09
4. A mild form of Hb S-β-thalassemia syndrome is assured in Sicilian patients by β+mutant IVS-I nt 6(T→C);European Journal of Haematology;2009-04-24
5. Modifier Genes and Oligogenic Disease;Journal of Nippon Medical School;2005
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