Thalassemia Intermedia Associated with Complex Interaction of Hb Beijing [α16(A14)Lys→Asn] and Hb E [β26(B8)Glu→Lys] with a Deletional α-Thalassemia-1 in a Thai Family
Authors:
- Supan FucharoenSFSupan Fucharoen
- Sunisa ChunpanichSCSunisa Chunpanich
- Kanokwan SanchaisuriyaKSKanokwan Sanchaisuriya
- Goonnapa FucharoenGFGoonnapa Fucharoen
- Naowarat KunyanoneNKNaowarat Kunyanone
- 1 January 2005
- journal article
- Published by Taylor & Francis in Hemoglobin
- Vol. 29 (1) , 77-83
Abstract
No abstract availableKeywords
This publication has 18 references indexed in Scilit:
- The Diverse Molecular Basis and Hematological Features of Hb H and AEBart’s Diseases in Northeast ThailandActa Haematologica, 2004
- A Simplified Screening for α-Thalassemia 1 (SEA Type) Using a Combination of a Modified Osmotic Fragility Test and a Direct PCR on Whole Blood Cell LysatesActa Haematologica, 2002
- Frequency Distribution and Haplotypic Heterogeneity of βE-Globin Gene among Eight Minority Groups of Northeast ThailandHuman Heredity, 2002
- Complex interactions of δβ hybrid haemoglobin (Hb Lepore‐Hollandia) Hb E (β26 G→A) and α+ thalassaemia in a Thai familyEuropean Journal of Haematology, 2002
- Hb Paksé [(α2) CODON 142 (TAA→TATOR Term→Tyr)] IN THAI PATIENTS WITH EABart's DISEASE AND Hb H DISEASEHemoglobin, 2002
- Hb E and α-Thalassemia; Variability in the Assembly of βEChain Containing TetramersHemoglobin, 1997
- Rapid and simultaneous non‐radioactive method for detecting α‐thalassemia 1 (SEA type) and Hb Constant Spring genesEuropean Journal of Haematology, 1994
- Hemoglobinopathies in Southeast AsiaHemoglobin, 1987
- Hemoglobin Beijing [α16(A14)Lys→Asn]: A New Fast-Moving Hemoglobin VariantHemoglobin, 1982
- Globin Chain Electrophoresis: a New Approach to the Determination of the Gγ/Aγ Ratio in Fetal Haemoglobin and to Studies of Globin SynthesisBritish Journal of Haematology, 1980