A Novel α-Thalassemia Nonsense Mutation on the α2-Globin Gene: HBA2: c.184A>T-Reference-Cited by-同舟云学术

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A Novel α-Thalassemia Nonsense Mutation on the α2-Globin Gene: HBA2: c.184A>T

Published:2017-11-02 Issue:4-6 Volume:41 Page:306-307
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Liang Yuan¹²,Peng Qi¹²,Li Miao³,Li Siping¹²,Li Wenrui¹²,Lu Xiaomei¹²^ORCID

Affiliation:

1. Department of Pediatrics, Dongguan Eighth People’s Hospital, Dongguan, Guangdong Province, People’s Republic of China;

2. Department of Medical and Molecular Genetics, Dongguan Institute of Pediatrics, Dongguan, Guangdong Province, People’s Republic of China;

3. Department of Gynecology and Obstetrics, Dongguan Eighth People’s Hospital, Dongguan, Guangdong Province, People’s Republic of China

Publisher

Informa UK Limited

Subject

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

Link

https://www.tandfonline.com/doi/pdf/10.1080/03630269.2017.1402027

Reference6 articles.

1. The Thalassaemia Syndromes

2. α-thalassaemia

3. First Case of a Compound Heterozygosity for Two Nondeletionalα-Thalassemia mutations, Hb Constant Spring and Hb Quong Sze

4. 2 α-Thalassaemia

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. First Report of Nondeletional Hb H Disease Caused by an α2-Globin Gene Mutation: HBA2: c.184A>T;Hemoglobin;2021-05-04

2. Next‐generation sequencing improves molecular epidemiological characterization of thalassemia in Chenzhou Region, P.R. China;Journal of Clinical Laboratory Analysis;2019-02-27

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