A Novel Pathogenic β-Thalassemia Mutation Identified at Codon 8 (HBB: c.27delG) in a Bangladeshi Family AcquiredDe Novo-Reference-Cited by-同舟云学术

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A Novel Pathogenic β-Thalassemia Mutation Identified at Codon 8 (HBB: c.27delG) in a Bangladeshi Family AcquiredDe Novo

Published:2019-05-04 Issue:3 Volume:43 Page:162-165
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Hasan Kazi N.¹^ORCID,Sufian Abu²,Mazumder Ashish K.²,Khaleque M. Abdul¹,Rahman Mizanur²,Akhteruzzaman Sharif³

Affiliation:

1. Department of Biochemistry and Microbiology, School of Health and Life Sciences, North South University, Block B, Dhaka, Bashundhara, Bangladesh;

2. DNA Solution Limited, West Panthapath, Dhaka, Bangladesh;

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

Publisher

Informa UK Limited

Subject

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

Link

https://www.tandfonline.com/doi/pdf/10.1080/03630269.2019.1638797

Reference20 articles.

1. Updates of the HbVar database of human hemoglobin variants and thalassemia mutations

2. 1 The population genetics of the haemoglobinopathies

3. Beta-thalassemia: from genotype to phenotype

4. De novo initiation codon mutation (ATG→ACG) of the β-globin gene causing β-thalassemia in a swiss family

5. Novel dominant β-thalassemia: Hb Boston-Kuwait [Codon 139/140(+T)]

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