Analysis of rare thalassemia caused by HS-40 regulatory site deletion
Author:
Affiliation:
1. Department of Medical Genetics, Liuzhou Maternal and Child Health Hospital, Liuzhou, People’s Republic of China
2. Department of Laboratory Medicine, Guangxi Zhuang Autonomous Region People’s Hospital, Nanning, People’s Republic of China
Publisher
Informa UK Limited
Subject
Hematology,Hematology
Link
https://www.tandfonline.com/doi/pdf/10.1080/16078454.2020.1799587
Reference16 articles.
1. α-thalassaemia
2. The prevalence and spectrum of and thalassaemia in Guangdong Province: implications for the future health burden and population screening
3. Molecular epidemiological survey of haemoglobinopathies in the Guangxi Zhuang Autonomous Region of southern China
4. Analysis of enhancer function of the HS-40 core sequence of the human alpha-globin cluster
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