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Hemoglobin
international journal for hemoglobin research
Volume 45, 2021 - Issue 5
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Original Articles

Spectrum of β-Thalassemia Mutations in Some Areas of Guangxi Zhuang Autonomous Region of Southern China: A Study on a Pediatric Population Aged 0–15 Years

Li-Fang Huanga Department of Pediatrics, The First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi Province, People’s Republic of China
,
Li-Li Yub Department of Pediatrics, Qinzhou Maternal and Child Health Care Hospital, Qinzhou, Guangxi Province, People’s Republic of China
,
Lauriane Nikuzea Department of Pediatrics, The First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi Province, People’s Republic of China
,
Sanjeev Singha Department of Pediatrics, The First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi Province, People’s Republic of China
,
Jin-Xia Jianga Department of Pediatrics, The First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi Province, People’s Republic of China
,
Jia-Li Jianga Department of Pediatrics, The First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi Province, People’s Republic of China
,
Yu-Ping Lia Department of Pediatrics, The First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi Province, People’s Republic of China
,
Yu-Hui Qina Department of Pediatrics, The First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi Province, People’s Republic of China
&
Hong-Ying Weia Department of Pediatrics, The First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi Province, People’s Republic of ChinaCorrespondence[email protected]
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Pages 318-321 | Received 01 Jul 2021, Accepted 19 Jan 2022, Published online: 06 May 2022

Citations (3)

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Read on this site (1)

Shao-Min Wu, Chan Li, Su-Ran Huang, Fan Jiang & Dong-Zhi Li. (2024) A 6-Year Follow-up of a Chinese Child with Homozygous β0-Thalaasemia and a Heterozygous KLF1 Mutation. Hemoglobin 48:1, pages 60-62.
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Articles from other publishers (2)

Guangli Wang, Huiping Deng, Peng Peng, Haiqing Zheng, Baodong Tian & Chunjiang Zhu. (2024) Compound heterozygosity for Southeast Asian hereditary persistence of fetal hemoglobin and β0-thalassemia results in thalassemia intermedia: Pedigree analysis and genetic research in a family from South China. A case report. Medicine 103:10, pages e37446.
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Haiyan Luo, Ting Huang, Qing Lu, Liuyang Zhang, Yonghua Xu, Yan Yang, Zhen Guo, Huizhen Yuan, Yinqin Shen, Shuhui Huang, Bicheng Yang, Yongyi Zou & Yanqiu Liu. (2022) Molecular prevalence of HBB-associated hemoglobinopathy among reproductive-age adults and the prenatal diagnosis in Jiangxi Province, southern central China. Frontiers in Genetics 13.
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