Identification of a Novel β-Globin Mutation (HBB: C.189_195delTCATGGC) in a Chinese Family-Reference-Cited by-同舟云学术

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Identification of a Novel β-Globin Mutation (HBB: C.189_195delTCATGGC) in a Chinese Family

Published:2016-07-03 Issue:4 Volume:40 Page:277-279
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

He Sheng,Lin Li,Wei Yuan,Chen Biyan,Yi Shang,Chen Qiuli,Qiu XiaoXia,Wei Hongwei,Li Guojian,Zheng Chenguang

Publisher

Informa UK Limited

Subject

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

Link

http://www.tandfonline.com/doi/pdf/10.1080/03630269.2016.1200073

Reference12 articles.

1. The prevalence and spectrum of and thalassaemia in Guangdong Province: implications for the future health burden and population screening

2. Molecular epidemiological survey of haemoglobinopathies in the Guangxi Zhuang Autonomous Region of southern China

3. A Novel 26 bp Deletion [HBB: c.20_45del26bp] in Exon 1 of the β-Globin Gene Causing β-Thalassemia Major

4. The Thalassaemia Syndromes

5. Molecular diagnosis of haemoglobin disorders

Cited by 2 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 of a new β-thalassaemia variant Term CD+32(HBB: c.32A>C) in two Chinese families;Journal of Clinical Pathology;2020-02-27

2. Hereditary xerocytosis - spectrum and clinical manifestations of variants in the PIEZO1 gene, including co-occurrence with a novel β-globin mutation;Blood Cells, Molecules, and Diseases;2020-02

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