The β-globin promoter −71 C>T mutation is a β+ thalassemic allele-Reference-Cited by-同舟云学术

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The β-globin promoter −71 C>T mutation is a β+ thalassemic allele

Published:2011-09-15 Issue:5 Volume:87 Page:457-460
ISSN:0902-4441
Container-title:European Journal of Haematology
language:en
Short-container-title:

Author:

Al Zadjali Shoaib,Wali Yasser,Al Lawatiya Fatma,Gravell David,AlKindi Salam,Al Falahi Kareema,Krishnamoorthy Rajagopal,Daar Shahina

Publisher

Wiley

Subject

Hematology,General Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1600-0609.2011.01687.x/fullpdf

Reference13 articles.

1. A community-based study of common hereditary blood disorders in Oman;Al-Riyami;East Mediterr Health J,2001

2. Forecasting hemoglobinopathy burden through neonatal screening in Omani neonates;Alkindi;Hemoglobin,2010

3. Rapid detection of alpha-thalassaemia deletions and alpha-globin gene triplication by multiplex polymerase chain reactions;Liu;Br J Haematol,2000

4. Genetic modifiers of b-thalassaemia;Thein;Haematologica,2005

5. First identification of a point mutation at position -83 (G>A) of the b-globin gene promoter;Cadet;Hemoglobin,2009

Cited by 12 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. Homozygous mild beta-thalassaemia promoter transversion −71 C>T HBB:c.-121 C>T;BMJ Case Reports;2023-04

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

3. Clinical and laboratory features of Hemoglobin La Desirade variant in association with sickle cell and alpha thalassemia genes;Mediterranean Journal of Hematology and Infectious Diseases;2020-12-31

4. Integrating ChIP-seq with other functional genomics data;Briefings in Functional Genomics;2018-03-01

5. The regulation of human globin promoters by CCAAT box elements and the recruitment of NF-Y;Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms;2017-05

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