Compound heterozygous β+ β0 mutation of HBB gene leading to β-thalassemia major in a Gujarati family

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Compound heterozygous β+ β0 mutation of HBB gene leading to β-thalassemia major in a Gujarati family — A case study

Published:2016-06 Issue: Volume:7 Page:51-53
ISSN:2214-4269
Container-title:Molecular Genetics and Metabolism Reports
language:en
Short-container-title:Molecular Genetics and Metabolism Reports

Author:

Chaudhary Spandan,Dhawan Dipali,Bagali Prashanth G.,S.Chaudhary Pooja,Chaudhary Abhinav,Singh Sanjay,Vudathala Srinivas

Publisher

Elsevier BV

Reference15 articles.

1. Changes in the epidemiology of thalassemia in North America: a new minority disease;Vichinsky;Pediatrics,2005

2. The Thalassaemia Syndromes;Weatherall,2008

3. A syllabus of thalassemia mutations;Huisman,1997

4. Thalassemia;Higgs,2011

5. Complications of β-thalassemia major in North America;Cunningham;Blood,2004

Cited by 4 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Subclinical atherosclerotic predictive value of inflammatory markers in thalassemia intermedia patients;Expert Review of Hematology;2021-07-03

2. Computational and drug target analysis of functional single nucleotide polymorphisms associated with Haemoglobin Subunit Beta (HBB) gene;Computers in Biology and Medicine;2020-10

3. Hematologic features of beta-globin gene mutation type (?o) with homozygous beta thalassemia;The Ukrainian Biochemical Journal;2018-06-22

4. Compound Heterozygosity of β-Thalassemia Traits of HBB Gene in a Family: A Case Report;International Journal of Human Genetics;2017-04-03

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