Silent β-Thalassemia Mutations at −101 (C>T) and −71 (C>T) and Their Coinheritance with the Sickle Cell Mutation in Bahrain-Reference-Cited by-同舟云学术

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Silent β-Thalassemia Mutations at −101 (C>T) and −71 (C>T) and Their Coinheritance with the Sickle Cell Mutation in Bahrain

Published:2013-04-15 Issue:4 Volume:37 Page:369-377
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Al Moamen Nabeel J.,Mahdi Fawzia,Salman Ebtihal,Ahmed Thabet,Abbas Ruqaya,Al Arrayed Shaikha,Sanad Hassan,Ahmed Al Alawi

Publisher

Informa UK Limited

Subject

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

Link

http://www.tandfonline.com/doi/pdf/10.3109/03630269.2013.785434

Reference19 articles.

1. Hemoglobinopathies and Glucose-6-Phosphate Dehydrogenase Deficiency in Hospital Births in Bahrain

2. Molecular Basis of beta-Thalassemia in Bahrain: An Epicenter for a Middle East Specific Mutationa

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1. Global distribution of β-thalassemia mutations: An update;Gene;2024-02

2. Unresolved laboratory issues of the heterozygous state of β-thalassemia: a literature review;Haematologica;2023-06-01

3. Significance of borderline HbA2 levels in β thalassemia carrier screening;Scientific Reports;2022-03-30

4. The Effect of HBB: c.-121C>T Variant [–71 (C>T)] on the β-Globin Promoter: Case Series Study;Hemoglobin;2021-07-04

5. Borderline HbA2 levels: Dilemma in diagnosis of beta-thalassemia carriers;Mutation Research/Reviews in Mutation Research;2021-07

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