Hb A2-Pasteur-Tunis [δ59(E3)Lys→Asn, AAG→AAC]: A New δ Chain Variant Detected by DNA Sequencing in a Tunisian Carrier of the Codon 39 (C→T) β0-Thalassemia Mutation-Reference-Cited by-同舟云学术

Hb A2-Pasteur-Tunis [δ59(E3)Lys→Asn, AAG→AAC]: A New δ Chain Variant Detected by DNA Sequencing in a Tunisian Carrier of the Codon 39 (C→T) β0-Thalassemia Mutation

Published:2007-01 Issue:1 Volume:31 Page:23-29
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Moumni Imen,Zorai Amine,Ben Daoued Bechir,Mosbahi Ikbel,Omar Souheil,Kaabachi Neziha,Dellagi Koussay,Abbes Salem

Publisher

Informa UK Limited

Subject

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

Link

http://www.tandfonline.com/doi/pdf/10.1080/03630260601057005

Reference13 articles.

1. MOLECULAR SPECTRUM OFα-THALASSEMIA IN TUNISIA: EPIDEMIOLOGY AND DETECTION AT BIRTH

2. Hb H Disease Among Tunisians: Molecular Characterization of α‐Thalassemia Determinants and Hematological Findings

3. Contribution to the Description of the β‐Thalassemia Spectrum in Tunisia and the Origin of Mutation Diversity

4. Molecular Basis of β‐Thalassemia in the Population of Tunisia

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2. Two new β+-thalassemia mutation [β -56 (G → C); HBBc. −106 G → C] and [β −83 (G → A); HBBc. −133 G → A] described among the Tunisian population;American Journal of Human Biology;2015-03-07

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4. A Study of δ-Globin Gene Mutations in the UK Population: Identification of Three Novel Variants and Development of a Novel DNA Test for Hb A′2;Hemoglobin;2014-03-06

5. A New δ Chain Variant, Hb A2-Tunis [δ46(CD5)Gly → Glu;HBD: c.140G>A], Observed in a Tunisian Family in Association with a Compound Heterozygosity for Hb C [β6(A3)Glu → Lys;HBB: c.19G>A] β0-Thalassemia [IVS-I-1 (β143, G>A);HBB: c.92+1G>A];Hemoglobin;2014-01-29