Thalassemia Intermedia Due to a Novel Mutation in the Second Intervening Sequence of the β-Globin Gene-Reference-Cited by-同舟云学术

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Thalassemia Intermedia Due to a Novel Mutation in the Second Intervening Sequence of the β-Globin Gene

Published:2007-01 Issue:4 Volume:31 Page:433-438
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Agouti Imane,Bennani Mohcine,Ahmed Abouyoub,Barakat Amina,Mohamed Khattab,Badens Catherine

Publisher

Informa UK Limited

Subject

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

Link

http://www.tandfonline.com/doi/pdf/10.1080/03630260701613210

Reference12 articles.

2. A simple salting out procedure for extracting DNA from human nucleated cells

3. DNA polymorphism and molecular pathology of the human globin gene clusters

4. A single tube multiplex PCR method to detect the common alpha + thalassemia alleles

5. Rapid analysis of -α3.7thalassaemia and αααanti 3.7triplication by enzymatic amplification analysis

Cited by 5 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. The Scope for Thalassemia Gene Therapy by Disruption of Aberrant Regulatory Elements;Journal of Clinical Medicine;2019-11-13

2. Characterization of Two Deep Intronic Variants on the β-Globin Gene with Inconsistent Interpretations of Clinical Significance;Hemoglobin;2018-03-04

3. The Rare Codon 24 (T>A) (β+) Mutation in Association with the Common Codon 39 (C> T) (β0) Mutation Causes Transfusion-Dependent β-Thalassemia in a Moroccan Patient;Hemoglobin;2009-01

4. High-density SNP genotyping to define β-globin locus haplotypes;Blood Cells, Molecules, and Diseases;2009-01

5. Molecular Basis of β-Thalassemia in Morocco: Possible Origins of the Molecular Heterogeneity;Genetic Testing;2008-12

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