Publication Cover
Hemoglobin
international journal for hemoglobin research
Volume 42, 2018 - Issue 3
161
Views
11
CrossRef citations to date
0
Altmetric
Original Article

Analysis of Gene Mutation Types of α- and β-Thalassemia in Fuzhou, Fujian Province in China

, , , , &
Pages 143-147 | Received 23 Apr 2018, Accepted 06 Jun 2018, Published online: 22 Oct 2018

References

  • Rosnah B, Rosline H, Zaidah AW, et al. Detection of common deletional α-thalassemia spectrum by molecular technique in Kelantan, northeastern Malaysia. ISRN Hematol. 2012;2012:462969.
  • He S, Li J, Li DM, et al. Molecular characterization of α- and β-thalassemia in the Yulin region of Southern China. Gene. 2018;655(1):61–64.
  • Hemminki K, Li X, Forsti A, et al. Thalassemia and sickle cell anemia in Swedish immigrants: genetic diseases have become global. SAGE Open Med. 2015;3:2050312115613097.
  • Yu X, Yang LY, Yang HT, et al. Molecular epidemiological investigation of thalassemia in the Chengdu Region, Sichuan Province, Southwest China. Hemoglobin. 2015;39(6):393–397.
  • Lai K, Huang G, Su L, He Y. The prevalence of thalassemia in mainland China: evidence from epidemiological surveys. Sci Rep. 2017;7(1):920–931.
  • Xiong F, Sun M, Zhang X, et al. Molecular epidemiological survey of haemoglobinopathies in the Guangxi Zhuang Autonomous Region of southern China. Clin Genet. 2010;78(2):139–148.
  • Zheng CG, Liu M, Du J, et al. Molecular spectrum of α- and β-globin gene mutations detected in the population of Guangxi Zhuang Autonomous Region, People's Republic of China. Hemoglobin. 2011;35(1):28–39.
  • Zheng X, Lin M, Yang H, et al. Molecular epidemiological characterization and health burden of thalassemias in the Chaoshan Region, People’s Republic of China. Hemoglobin. 2016;40(2):138–142.
  • He S, Qin Q, Yi S, et al. Prevalence and genetic analysis of α- and β-thalassemia in Baise region, a multi-ethnic region in southern China. Gene. 2017;619(1):71–75.
  • Yao H, Chen X, Lin L, et al. The spectrum of α- and β-thalassemia mutations of the Li people in Hainan Province of China. Blood Cells Mol Dis. 2014;53(1-2):16–20.
  • Raffield LM, Ulirsch JC, Naik RP. Common α-globin variants modify hematologic and other clinical phenotypes in sickle cell trait and disease. Plos Genet. 2018;14(3):e1007293.
  • Harteveld CL, Higgs DR. α-Thalassaemia. Orphanet J Rare Dis. 2010;5:13.
  • Chen PQ, Liang QN, Huang TS, et al. A simple, rapid, and highly sensitive electrochemical DNA sensor for the detection of α- and β-thalassemia in China. J Clin Lab Anal. 2016;30(5):719–726.
  • He J, Zeng XH, Xu YM, et al. Gene analysis of thalassemia in Han and Dai ethnic childbearing-aged population of Chinese Yunnan Province. Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2016;24(1):150–156.
  • Hu ZH, Chen JY, Shi YL, et al. Molecular epidemiological analysis of α- and β-thalassemia in Fujian province. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2010;10(4):7439–7440.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.