Molecular Mechanisms Underlying Thalassemia Intermedia in Iran-Reference-Cited by-同舟云学术

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Molecular Mechanisms Underlying Thalassemia Intermedia in Iran

Published:2008-12 Issue:4 Volume:12 Page:549-556
ISSN:1090-6576
Container-title:Genetic Testing
language:en
Short-container-title:Genetic Testing

Author:

Neishabury Maryam¹,Azarkeivan Azita²,Oberkanins Christian³,Esteghamat Fatemehsadat¹,Amirizadeh Naser²,Najmabadi Hossein¹⁴

Affiliation:

1. Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.

2. Thalassemia Clinic and Research Center, Iranian Blood Transfusion Organization (IBTO), Tehran, Iran.

3. ViennaLab Diagnostics GmbH, Vienna, Austria.

4. Kariminejad and Najmabadi Pathology and Genetics Center, Tehran, Iran.

Publisher

Mary Ann Liebert Inc

Subject

Genetics(clinical)

Link

http://www.liebertpub.com/doi/pdf/10.1089/gte.2008.0018

Reference28 articles.

1. A novel mechanism for thalassaemia intermedia

2. Molecular pathology of thalassemia intermedia

3. Severe inclusion body β-thalassaemia with haemolysis in a patient double heterozygous for β°-thalassaemia and quadruplicated α-globin gene arrangement of the anti-4.2 type

4. Modern treatment of thalassaemia intermedia

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1. Molecular and geographical heterogeneity of hemoglobinopathy mutations in Azerbaijanian populations;Annals of Human Genetics;2019-11-21

2. Genotype-phenotype association analysis identifies the role of α globin genes in modulating disease severity of β thalassaemia intermedia in Sri Lanka;Scientific Reports;2019-07-12

3. Molecular characterization of β-thalassemia intermedia in the West Bank, Palestine;BMC Hematology;2019-02-18

4. Presence of the IVS-I-6-Mutated Allele in Beta-Thalassemia Major Patients Correlates with Extramedullary Hematopoiesis Incidence;Acta Haematologica;2017

5. Electromobility Shift Assay Reveals Evidence in Favor of Allele-Specific Binding of RUNX1 to the 5′ Hypersensitive Site 4-Locus Control Region;Hemoglobin;2016-07-03

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