HB Seal Rock [(α2)142 Term→glu, Codon 142 TAA→GAA]: An Extended α Chain Variant Associated with Anemia, Microcytosis, and α-Thalassemia-2 (-3.7 KB)-Reference-Cited by-同舟云学术

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HB Seal Rock [(α2)142 Term→glu, Codon 142 TAA→GAA]: An Extended α Chain Variant Associated with Anemia, Microcytosis, and α-Thalassemia-2 (-3.7 KB)

Published:1997-01 Issue:4 Volume:21 Page:331-344
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Merritt D.,Jones R. T.,Head C.,Thibodeau S. N.,Fairbanks V. F.,Steinberg M. H.,Coleman M. B.,Rodgers G. P.

Publisher

Informa UK Limited

Subject

Biochemistry (medical),Clinical Biochemistry,Genetics (clinical),Hematology

Link

http://www.tandfonline.com/doi/pdf/10.3109/03630269709000666

Reference27 articles.

1. HÆMOGLOBIN-H DISEASE DUE TO A UNIQUE HÆMOGLOBIN VARIANT WITH AN ELONGATED α-CHAIN

2. Haemoglobin Constant Spring—A Chain Termination Mutant ?

3. An Unusual Hemoglobin Anomaly and Its Relation to α-Thalassemia and Hemoglobin-H Disease

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1. Molecular Heterogeneity of Hb H Disease in India;Thalassemia Reports;2022-07-06

2. Detection of hemoglobin Kinshasa by a capillary electrophoresis method;Clinica Chimica Acta;2022-06

3. Two α1-Globin Gene Point Mutations Causing Severe Hb H Disease;Hemoglobin;2017-11-02

4. Five Rare β Globin Chain Hemoglobin Variants in India;Indian Journal of Hematology and Blood Transfusion;2016-04-12

5. Diagnostic pitfalls of less well recognized HbH disease;Blood Cells, Molecules, and Diseases;2015-12

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