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Two novel copy number variations involving the α-globin gene cluster on chromosome 16 cause thalassemia in two Chinese families

Crossref DOI link: https://doi.org/10.1007/s00438-016-1193-0

Published Online: 2016-03-21

Published Print: 2016-06

Update policy: https://doi.org/10.1007/springer_crossmark_policy

Authors

Hu, Lingling

Shang, Xuan

Yi, Sheng

Cai, Ren

Li, Zhetao

Liu, Cuixian

Liang, Yidan

Cai, Decheng

Zhang, Feng

Xu, Xiangmin
Funding

Funding for this research was provided by:

National Natural Science Foundation of China (81200403, 81360091)

Science and Technology Program of Guangzhou (201300000095)

the Special Project on the Integration of Industry, Education and Research of Guangdong Province (2012B091000148)
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Article History

Received: 6 January 2016

Accepted: 29 February 2016

First Online: 21 March 2016

Compliance with ethical standards

:

: The authors declare that they have no conflict of interest.

: All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional research committee and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards.

: Informed consent was obtained from all individual participants included in the study.