An α-Thalassemic Hemoglobinopathy: Homozygosity for the Hb Agrinio α2-Globin Chain Variant-Reference-Cited by-同舟云学术

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An α-Thalassemic Hemoglobinopathy: Homozygosity for the Hb Agrinio α2-Globin Chain Variant

Published:1998-01 Issue:3 Volume:22 Page:209-215
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Traeger-Synodinos J.,Metaxotou-Mavromati A.,Kanavakis E.,Vrettou C.,Papassotiriou I.,Michael Th.,Kattamis C.

Publisher

Informa UK Limited

Subject

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

Link

http://www.tandfonline.com/doi/pdf/10.3109/03630269809113135

Reference20 articles.

1. Hb adana or α259(E8)Gly→Aspβ2, A severely unstable α1-globin variant, observed in combination with the -(α)20.5 KB α-thal-1 deletion in two Turkish patients

2. A base substitution (T→C) in codon 29 of the α2-globin gene causes α thalassaemia

3. Haemoglobin Tunis-Bizerte: a new a globin 129 Leu–> Pro unstable variant with thalassaemic phenotype

Cited by 14 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. Concomitant Presence of Hb Agrinio and - -Med Deletion in a Greek Male Patient with Hemoglobinopathy H: More Severe Phenotype and Literature Review;Hematology Reports;2023-08-08

2. First Cases of Hb Agrinio Described in Patients from the Republic of Macedonia;Hemoglobin;2017-11-02

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

4. Hb Dartmouth (HBA2: c.200T>C): An α2-Globin Gene Associated with Hb H Disease in One Homozygous Patient;Hemoglobin;2015-05-04

5. Study of Three Families with Hb Agrinio [α29(B10)Leu→Pro, CTG>CCG (α2)] in the Spanish Population: Three Homozygous Cases;Hemoglobin;2012-08

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