Severe β0 thalassemia/hemoglobin E disease caused by de novo 22-base pair duplication in the paternal allele of β globin gene
Author:
Publisher
Wiley
Subject
Hematology
Reference9 articles.
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2. Update in the genetics of thalassemia: What clinicians need to know;Best Practice & Research Clinical Obstetrics & Gynaecology;2017-02
3. Molecular mechanisms of a novel β-thalassaemia mutation due to the duplication of tetranucleotide ‘AGCT’ at the junction IVS-II/exon 3;Annals of Hematology;2012-07-24
4. A novel de novo BRCA1 mutation in a Chinese woman with early onset breast cancer;Familial Cancer;2011-03-15
5. Hemoglobin H disease due to a de novo mutation at the α2-globin gene and an inherited common α-thalassemia deletion found in a Chinese boy;Blood Cells, Molecules, and Diseases;2010-10
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