Structural and functional studies on hemoglobin Bethesda (α2β2145 His), a variant associated with compensatory erythrocytosis-Reference-Cited by-同舟云学术

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Structural and functional studies on hemoglobin Bethesda (α2β2145 His), a variant associated with compensatory erythrocytosis

Published:1972-09-01 Issue:9 Volume:51 Page:2299-2309
ISSN:0021-9738
Container-title:Journal of Clinical Investigation
language:en
Short-container-title:J. Clin. Invest.

Author:

Bunn H. Franklin,Bradley Thomas B.,Davis William E.,Drysdale James W.,Burke John F.,Beck William S.,Laver Myron B.

Publisher

American Society for Clinical Investigation

Subject

General Medicine

Cited by 32 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. Systematic Assessment of Protein C-Termini Mutated in Human Disorders;Biomolecules;2023-02-12

2. Hb Angers: A new α2‐globin variant [α2 (140)(HC2) Tyr → Ser; HBA2 : C.422 A>C] with increased oxygen affinity leading to erythrocytosis;International Journal of Laboratory Hematology;2020-11-20

3. Hemoglobin: Structure, Function and Allostery;Subcellular Biochemistry;2020

4. A Japanese Family with Congenital Erythrocytosis Caused by Haemoglobin Bethesda;Internal Medicine;2015

5. Automated Analysis of Hemoglobin Variants Using NanoLC–MS and Customized Databases;Journal of Proteome Research;2013-06-06

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