Mutant Hemoglobins Having Elongated Chains
Author:
Publisher
Informa UK Limited
Subject
Biochemistry (medical),Clinical Biochemistry,Genetics (clinical),Hematology
Link
http://www.tandfonline.com/doi/pdf/10.3109/03630267808999185
Reference45 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. HEMOGLOBIN CONSTANT SPRING, AN UNUSUAL ?-CHAIN VARIANT INVOLVED IN THE ETIOLOGY OF HEMOGLOBIN H DISEASE
4. Inheritance of Haemoglobin H Disease
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1. Studies of the Oxidation of Ethanol to Acetaldehyde by Oxyhemoglobin Using Fluorigenic High-Performance Liquid Chromatography;Alcoholism: Clinical and Experimental Research;1994-10
2. Hb Catonsville (glutamic acid inserted between Pro-37(C2)α and Thr-38(C3)α);Journal of Biological Chemistry;1989-12
3. Structural and functional studies of Hemoglobin Wayne: An elongated α-chain variant;Journal of Molecular Biology;1984-12
4. Hemoglobin Analysis and Hemoglobinopathies;Clinical Biochemistry;1984
5. Haemoglobin Constant Spring has an unstable α chain messenger RNA;British Journal of Haematology;1982-07
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