Mutation Analysis of theHBBGene in Selected Bangladeshi β-Thalassemic Individuals: Presence of Rare Mutations-Reference-Cited by-同舟云学术

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Mutation Analysis of theHBBGene in Selected Bangladeshi β-Thalassemic Individuals: Presence of Rare Mutations

Published:2010-06 Issue:3 Volume:14 Page:299-302
ISSN:1945-0265
Container-title:Genetic Testing and Molecular Biomarkers
language:en
Short-container-title:Genetic Testing and Molecular Biomarkers

Author:

Ayub Mustak Ibn¹,Moosa Mahdi Muhammad¹,Sarwardi Golam²,Khan Waqar²,Khan Haseena³,Yeasmin Sabina¹

Affiliation:

1. Department of Genetic Engineering and Biotechnology, University of Dhaka, Dhaka, Bangladesh.

2. Department of Clinical Pathology and Biochemistry, Dhaka Shishu Hospital, Dhaka, Bangladesh.

3. Department of Biochemistry and Molecular Biology, University of Dhaka, Dhaka, Bangladesh.

Publisher

Mary Ann Liebert Inc

Subject

Genetics (clinical),General Medicine

Link

http://www.liebertpub.com/doi/pdf/10.1089/gtmb.2009.0160

Reference25 articles.

1. Thalassemia in Iran

2. A new mutation at IVS1 nt 2(T----A), in beta-thalassemia from Algeria

3. The peculiar spectrum of ?-thalassemia genes in Tunisia

4. DNAzol®: A Reagent for the Rapid Isolation of Genomic DNA

5. HPLC studies in hemoglobinopathies

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1. β-Thalassemia in Bangladesh: Current Status and Future Perspectives;Thalassemia Reports;2024-07-08

2. Case report and characterization of a Brazilian family with a rare hemoglobin variant—Hb Maputo;Hematology, Transfusion and Cell Therapy;2024-04

3. α- and β-Globin Gene Mutations in Individuals with Hemoglobinopathies in the Chattogram and Sylhet Regions of Bangladesh;Hemoglobin;2023-01-02

4. Direct sequencing of β-globin gene reveals a rare combination of two exonic and two intronic variants in a β-thalassemia major patient: a case report;Journal of Medical Case Reports;2022-10-09

5. Tracing the Indian Population Ancestry by cis-linked Mutations in HBB Gene;2021-04-21

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