Pedigree Analysis of Nonhomologous Sequence Recombination of HBA1 and HBA2 Genes-Reference-Cited by-同舟云学术

Pedigree Analysis of Nonhomologous Sequence Recombination of HBA1 and HBA2 Genes

Published:2020-08-19 Issue:5 Volume:44 Page:329-333
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Luo Shi-Qiang¹²,Chen Xing-Yuan³,Tang Ning¹²,Huang Jun¹²,Zhong Qing-Yan¹²,Cai Ren¹²,Yan Ti-Zhen¹²

Affiliation:

1. Department of Medical Genetics, Liuzhou Maternity and Child Healthcare Hospital, Liuzhou, Guangxi Zhuang Autonomous Region, People’s Republic of China

2. Institute of Reproduction and Genetics, Liuzhou Maternity and Child Healthcare Hospital, Liuzhou, Guangxi Zhuang Autonomous Region, People’s Republic of China

3. Department of Laboratory Medicine, The People’s Hospital of Guangxi Zhuang Autonomous Region, Nanning, Guangxi Zhuang Autonomous Region, People’s Republic of China

Funder

National Natural Science Foundation of China

Liuzhou Science and Technology Innovation Capability and Conditions Construction Project

Scientific Research Fund of the Health and Family Planning Commission of the Guangxi Zhuang Autonomous Region, Nanning, Guangxi, People’s Republic of China

Publisher

Informa UK Limited

Subject

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

Link

https://www.tandfonline.com/doi/pdf/10.1080/03630269.2020.1807355

Reference10 articles.

1. Higgs DR. Molecular mechanisms of α thalassemia. In: Steinberg MH, Forget BG, Higgs DR, editors. Disorders of Hemoglobin Genetics, Pathophysiology, and Clinical Management, 1st ed. Cambridge (NY, USA): Cambridge University Press; 2001. p. 405–430.

2. α-thalassaemia

3. Boundaries of gene conversion within the duplicated human alpha-globin genes. Concerted evolution by segmental recombination.

4. A novel HBA2 gene conversion in cis or trans: “α12 allele” in a Saudi population

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