A Hb J cape town homozygote - association of Hb J cape town and alpha-thalassaemia
Author:
Publisher
Wiley
Subject
Cell Biology,Genetics,Molecular Biology,Biochemistry,Structural Biology,Biophysics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1016/0014-5793(78)80429-3/fullpdf
Reference16 articles.
1. Differences between - and -Chain Mutants of Human Haemoglobin and between - and -Thalassaemia. Possible Duplication of the -Chain Gene
2. Homozygous Hb J Tongariki: Evidence for Only One Alpha Chain Structural Locus in Melanesians
3. VARIOUS ASPECTS OF?-THALASSEMIA
4. Haemoglobin J Tongariki is associated with α thalassaemia
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1. In SilicoAnalysis of the Effects of Point Mutations on α-Globin: Implications for α-Thalassemia;Hemoglobin;2020-03-03
2. The haematological puzzle of Hb J Cape Town is partly solved;British Journal of Haematology;2008-03-12
3. Hb J-CAPE TOWN [α92(FG4)Arg→Gln (α1), CGG→CAG] in Southern Italy Found in a Patient with Erythrocytosis;Hemoglobin;2007-01
4. Hb Chesapeake [α92 (Fg 4) Arg → Leu] and Hb J Cape Town [α92 (Fg 4) Arg → Gln] First Discovered in Japanese;Hemoglobin;1983-01
5. Identification of hemoglobin G-Philadelphia (α68 Asn→Lys) and homoglonin matsue-oki (α75 Asp→Asn) in a black infant;Biochimica et Biophysica Acta (BBA) - Protein Structure and Molecular Enzymology;1982-10
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