Prevalence and genetic analysis of α- and β-thalassemia in Baise region, a multi-ethnic region in southern China-Reference-Cited by-同舟云学术

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Prevalence and genetic analysis of α- and β-thalassemia in Baise region, a multi-ethnic region in southern China

Published:2017-07 Issue: Volume:619 Page:71-75
ISSN:0378-1119
Container-title:Gene
language:en
Short-container-title:Gene

Author:

He Sheng,Qin Qian,Yi Shang,Wei Yuan,Lin Li,Chen Shaoke,Deng Jianping,Xu Xianmin,Zheng Chenguang,Chen Biyan

Funder

Guangxi science and Technology Department

Health Department of Guangxi Province

Natural Science Foundation of China

Publisher

Elsevier BV

Subject

Genetics,General Medicine

Reference28 articles.

1. Single-tube multiplex-PCR screen for common deletional determinants of alpha-thalassaemia;Chong;Blood,2000

2. Characterization of two deletions that remove the entire human zeta-alpha globin. Gent complex (- -THAI and - -FIL);Fischel-Ghodsian;Br. J. Hemeatol.,1988

3. Updates of the HbVar database of human hemoglobin variants and thalassemia mutations;Giardine;Nucleic Acids Res.,2014

4. Hb Var: A relational database of human hemoglobin variants and thalassemia mutations at the globin gene server;Hardison;Hum. Mutat.,2002

5. First description of a β-thalassemia mutation,-86 (C>G) (HBB:c.-136C>G), in a Chinese family;He;Hemoglobin,2015

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5. Differential diagnosis between iron deficiency anemia and thalassemia trait-induced anemia;Journal of Dental Sciences;2023-10

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