Hb SITIA [β128(H6)Ala→Val]: AN UNSTABLE VARIANT WITH A SUBSTITUTION IN THE α1β1 INTERFACE-Reference-Cited by-同舟云学术

Hb SITIA [β128(H6)Ala→Val]: AN UNSTABLE VARIANT WITH A SUBSTITUTION IN THE α1β1 INTERFACE

Published:2001-01 Issue:1 Volume:25 Page:45-56
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Papassotiriou Ioannis,Traeger-Synodinos Joanne,Promé Danielle,Kister Jean,Vrettou Christina,Xaidara Athina,Marden Michael,Stamoulakatou Alexandra,Wajcman Henri,Kanavakis Emmanuel

Publisher

Informa UK Limited

Subject

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

Link

http://www.tandfonline.com/doi/pdf/10.1081/HEM-100103069

Reference19 articles.

1. Location of Amino Acid Residues in Human Deoxy Hemoglobin

2. Association of unstable hemoglobin variants and heterozygous ?-thalassemia: Example of a new variant Hb acharnes or [?53(D4) Ala ? Thr]

3. Gamma Chain Heterogeneity: Determination of Hb F Composition by Perfusion Chromatography

Cited by 4 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. Observation of a Rare Hemoglobin Variant [Hb Lulu Island, β107(G9)Gly→Asp, GGC→GAC] Co-Inherited With a β+-Thalassemia Mutation [IVS-I-110 (G→A)] or in the Heterozygous State in a Greek-Albanian Family;Hemoglobin;2006-01

2. The homozygous state for Hb Crete [β129 (H7) Ala→Pro] is associated with a complex phenotype including erythrocytosis and functional anemia;Blood Cells, Molecules, and Diseases;2005-05

3. Rare thalassemic syndrome caused by interaction of Hb Questembert (α1 codon 131, TCT>CCT, Ser>Pro) with an α-thalassemia-2 deletion: implications for diagnosis and management;Blood Cells, Molecules, and Diseases;2004-02

4. Hb MONT SAINT AIGNAN [β128(H6)Ala → Pro]: A NEW UNSTABLE VARIANT LEADING TO CHRONIC MICROCYTIC ANEMIA;Hemoglobin;2001-01