Hemoglobin Evanston (alpha 14 Trp----Arg). An unstable alpha-chain variant expressed as alpha-thalassemia.-Reference-Cited by-同舟云学术

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Hemoglobin Evanston (alpha 14 Trp----Arg). An unstable alpha-chain variant expressed as alpha-thalassemia.

Published:1984-06-01 Issue:6 Volume:73 Page:1740-1749
ISSN:0021-9738
Container-title:Journal of Clinical Investigation
language:en
Short-container-title:J. Clin. Invest.

Author:

Honig G R,Shamsuddin M,Vida L N,Mompoint M,Valcourt E,Bowie L J,Jones E C,Powers P A,Spritz R A,Guis M

Publisher

American Society for Clinical Investigation

Subject

General Medicine

Cited by 35 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. Exploration de l’hémolyse associée à la drépanocytose et perspectives thérapeutiques spécifiques;La Revue de Médecine Interne;2023-11

2. Hb Dapu (HBA2: c.52G > T): A Novel Nondeletional α-Thalassemia Mutation;Hemoglobin;2016-06-03

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

4. Hb Souli, a 6 bp In-Frame Deletion on theHBA2Gene (HBA2: c.[41-46delCCTGGG]) Leads toα-Thalassemia Intermedia, When inTransto a Singleα-Globin Gene Deletion;Hemoglobin;2014-12-05

5. Alpha Thalassaemia and extended alpha globin genes in Sri Lanka;Blood Cells, Molecules, and Diseases;2013-02

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