HB E [β26(B8)GLU→LYS] in a Czechoslovakian Family
Author:
Publisher
Informa UK Limited
Subject
Biochemistry (medical),Clinical Biochemistry,Genetics (clinical),Hematology
Link
http://www.tandfonline.com/doi/pdf/10.3109/03630269109072494
Reference5 articles.
1. Hemoglobin E trait reexamined: a cause of microcytosis and erythrocytosis
2. Hb-linköping (β36 Pro → Thr): a new hemoglobin mutant characterized by reversed-phase high-performance liquid chromatography
3. Separation of the α and β-Chains of Human Haemoglobin
4. On-line HPLC analysis of PTH-amino acids derived from Edman degradation of proteins and peptides: Optical sensor controlled sample injection
Cited by 4 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Hb Nottingham or α2β2 98 (FG5) Val→Gly in a Czech child;Annals of Hematology;1994-08
2. Molecular characterization of β-thalassemia in Czechoslovakia;Human Genetics;1992-02
3. A Czechoslovakian teenager with Hb E-β∘-thalassemia [IVS-I-1 (G → A)] complicated by the presence of an α-globin gene triplication;Annals of Hematology;1991-07
4. HB Köln or α2β298(FG5)VAL→MET in a Czechoslovakian Family;Hemoglobin;1991-01
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