An IVS1-116 (A→G) acceptor splice site mutation in the α2 globin gene causing α+ thalassaemia in two Dutch families
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1365-2141.1996.d01-1926.x/fullpdf
Cited by 23 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. Identification and Molecular Analysis of Putative Self-Incompatibility Ribonuclease Alleles in an Extreme Polyploid Species, Prunus laurocerasus L.;Frontiers in Plant Science;2021-09-23
2. A cytosine-rich splice regulatory determinant enforces functional processing of the human α-globin gene transcript;Blood;2019-05-23
3. First Report of a Case with Nondeletional Hb H Disease Caused by IVS-I-116 (A>G) of the α2-Globin Gene;Hemoglobin;2018-11-02
4. A Unique Interaction of IVS-I-1 (G>A) (HBA2: c.95+1G>A) with Hb Adana (HBA2: c.179G>A) Presenting as Transfusion-Dependent α-Thalassemia;Hemoglobin;2018-07-04
5. Molecular diagnosis of α-thalassemia in a multiethnic population;European Journal of Haematology;2017-04-06
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