Identification of a Novel β-Thalassemia Mutation at Codon 130 (+T) (HBB: c.391insT) in Han Chinese-Reference-Cited by-同舟云学术

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Identification of a Novel β-Thalassemia Mutation at Codon 130 (+T) (HBB: c.391insT) in Han Chinese

Published:2021-01-02 Issue:1 Volume:45 Page:46-48
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Wang Wen-Juan¹,Ding Zi-Xuan¹,Zhang Hui-Min¹,Tao Ting-Ting¹,Chen Su-Ning¹,Xi Ling²

Affiliation:

1. Collaborative Innovation Center of Hematology, The First Affiliated Hospital of Soochow University, Jiangsu Institute of Hematology, Key Laboratory of Thrombosis and Hemostasis of Ministry of Health, Suzhou, Jiangsu, PR China

2. Department of Gynecology and Obstetrics, The First Affiliated Hospital of Soochow University, Suzhou, Jiangsu, PR China

Publisher

Informa UK Limited

Subject

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

Link

https://www.tandfonline.com/doi/pdf/10.1080/03630269.2020.1862183

Reference9 articles.

1. Updates of the HbVar database of human hemoglobin variants and thalassemia mutations

2. A Novel β-Thalassemia Mutation in a Chinese family: IVS-II-203-205 (TCT>CC) (HBB: c.315+203TCT>CC)

3. Characteristics and distribution of ? thalassemia haplotypes in South China

4. Identification of Two Novelβ-Thalassemia Mutations (HBB: c.335-346del andHBB: c.108 C > G) in Han Chinese

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1. Alterations in trace elements and cation profiles in transfusion-dependent thalassemia patients;Transfusion and Apheresis Science;2024-08

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