Homozygosity for a Rare β0-Thalassemia Mutation [Frameshift Codons 25/26 (+T)] Causes β-Thalassemia Intermedia in an Iranian Family-Reference-Cited by-同舟云学术

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Homozygosity for a Rare β0-Thalassemia Mutation [Frameshift Codons 25/26 (+T)] Causes β-Thalassemia Intermedia in an Iranian Family

Published:2009-01 Issue:1 Volume:33 Page:75-80
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Haghi Mehdi,Hosseinpour Feizi Abbas A.,Harteveld Cornelis L.,Pouladi Nasser,Hosseinpour Feizi Mohammad A.

Publisher

Informa UK Limited

Subject

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

Link

http://www.tandfonline.com/doi/pdf/10.1080/03630260802683377

Reference18 articles.

1. Relationship between the severity of β-thalassaemia syndromes and the number of alleviating mutations

2. Detection of a Rare β-Globin Nonsense Mutation [Codon 59 (AAG→TAG)] in an Italian Family

3. The -158 site 5' to the G gamma gene and G gamma expression

4. THE TRIPLICATED ALPHA-GENE LOCUS AND HETEROZYGOUS BETA THALASSAEMIA: A CASE OF THALASSAEMIA INTERMEDIA

5. Effect of α-Gene Numbers on the Expression of β-Thalassemia intermedia, β-Thalassemia and (δβ)⁰-Thalassemia Traits

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1. The effect of aqueous extract of Iranian oak (Quercus brantii) on antioxidant capacity and oxidative stress in beta-thalassemia patients: Randomized controlled trial;Clinical Nutrition ESPEN;2024-06

2. Rare and New Mutations of B-Globin in Azari Population of Iran, a Considerable Diversity;Balkan Journal of Medical Genetics;2022-12-01

3. Diagnosis and prevention of thalassemia;Critical Reviews in Clinical Laboratory Sciences;2013-11

4. Prevalence of Xmnl Gγ polymorphism in Egyptian patients with β-thalassemia major;Annals of Saudi Medicine;2012-09

5. The expanding spectrum of thalassemia intermedia;Hematology;2009-12

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