A case of non-β-globin gene linked β thalassaemia in a Dutch family with two additional α-gene defects: the common −α3·7deletion and the rare IVS1-116 (A → G) acceptor splice site mutation-Reference-Cited by-同舟云学术

A case of non-β-globin gene linked β thalassaemia in a Dutch family with two additional α-gene defects: the common −α3·7deletion and the rare IVS1-116 (A → G) acceptor splice site mutation

Published:1998-11 Issue:2 Volume:103 Page:370-376
ISSN:0007-1048
Container-title:British Journal of Haematology
language:en
Short-container-title:British Journal of Haematology

Author:

Giordano ,Harteveld ,Haak ,Batelaan ,Van Delft ,Plug ,Emonts ,Zanardini ,Bernini

Publisher

Wiley

Subject

Hematology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1365-2141.1998.00999.x/fullpdf

Reference27 articles.

1. Rapid estimation of haemoglobin A2 by DEAE chromatography;Bernini;Biochemical Genetics,1969

2. Estimation of small percentages of foetal haemoglobin;Betke;Nature,1959

3. The mechanism of removal of leucocytes by cellulose columns;Beutler;Blood Cells,1986

4. Analyses of β-thalassemia mutant DNA interaction with erythroid Krüppel-like factor (EKLF), and erythroid cell-specific transcription factor;Feng;Journal of Biological Chemistry,1994

5. Heterozygous β-thalassemia with thalassemia intermedia phenotype;Gasperini;American Journal of Hematology,1988

Cited by 6 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. α, β, δ and γ thalassaemias and related conditions;Haemoglobinopathy Diagnosis;2020-02-28

2. Diverse hematological phenotypes of β-thalassemia carriers;Annals of the New York Academy of Sciences;2016-03

3. The genetic heterogeneity of β-globin gene defects in Sicily reflects the historic population migrations of the island;Blood Cells, Molecules, and Diseases;2011-04

4. Comprehensive Spectrum of the β-Thalassemia Mutations in Khuzestan, Southwest Iran;Hemoglobin;2010-09-20

5. Segmental duplications involving the α-globin gene cluster are causing β-thalassemia intermedia phenotypes in β-thalassemia heterozygous patients;Blood Cells, Molecules, and Diseases;2008-05