REPORT OF NEW ALLELES AND ANTIGENS
A novel A allele with c.689G>T mutation identified in a Chinese individual
Wenhui Ma,
Wenhui Ma
Institute for Transfusion Medicine, Qingdao Blood Center, Qingdao, Shandong, China
Search for more papers by this author Zhihui Feng,
Zhihui Feng
Institute for Transfusion Medicine, Qingdao Blood Center, Qingdao, Shandong, China
Search for more papers by this author Bin Hu,
Bin Hu
Institute for Transfusion Medicine, Qingdao Blood Center, Qingdao, Shandong, China
Search for more papers by this author Bin Han,
Bin Han
Institute for Transfusion Medicine, Qingdao Blood Center, Qingdao, Shandong, China
Search for more papers by this author Shuxian Jiao,
Corresponding Author
Shuxian Jiao
Institute for Transfusion Medicine, Qingdao Blood Center, Qingdao, Shandong, China
Address reprint requests to: Shuxian Jiao, PhD, Longde Road 9#, Qingdao, Shandong Province 266071, China; e-mail:
[email protected].
Search for more papers by this author
Wenhui Ma,
Wenhui Ma
Institute for Transfusion Medicine, Qingdao Blood Center, Qingdao, Shandong, China
Search for more papers by this author Zhihui Feng,
Zhihui Feng
Institute for Transfusion Medicine, Qingdao Blood Center, Qingdao, Shandong, China
Search for more papers by this author Bin Hu,
Bin Hu
Institute for Transfusion Medicine, Qingdao Blood Center, Qingdao, Shandong, China
Search for more papers by this author Bin Han,
Bin Han
Institute for Transfusion Medicine, Qingdao Blood Center, Qingdao, Shandong, China
Search for more papers by this author Shuxian Jiao,
Corresponding Author
Shuxian Jiao
Institute for Transfusion Medicine, Qingdao Blood Center, Qingdao, Shandong, China
Address reprint requests to: Shuxian Jiao, PhD, Longde Road 9#, Qingdao, Shandong Province 266071, China; e-mail:
[email protected].
Search for more papers by this author
First published: 24 August 2018
No abstract is available for this article.
CONFLICT OF INTEREST
The authors have disclosed no conflicts of interest.
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Table S1. Amplification and sequencing primers |
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REFERENCES
- 1Ogasawara K, Yabe R, Uchikawa M, et al. Molecular genetic analysis of variant phenotypes of the ABO blood group system. Blood 1996; 88: 2732-7.
- 2Sunyaev S, Ramensky V, Koch I, et al. Prediction of deleterious human alleles. Hum Mol Genet 2001; 10: 591-7.
