Identification of a novel A4GALT*299A allele associated with the rare p phenotype in one Chinese family

TransfusionEarly View ONE-PAGE REPORT OF NEW ALLELES OR ANTIGENS Identification of a novel A4GALT*299A allele associated with the rare p phenotype in one Chinese family Chunyan Mo, Chunyan Mo orcid.org/0009-0003-4943-9524 Institute of Clinical Blood Transfusion, Guangzhou Blood Center, Guangzhou, ChinaSearch for more papers by this authorShuangshuang Jia, Shuangshuang Jia orcid.org/0000-0002-0092-8576 Institute of Clinical Blood Transfusion, Guangzhou Blood Center, Guangzhou, ChinaSearch for more papers by this authorGuangping Luo, Guangping Luo Institute of Clinical Blood Transfusion, Guangzhou Blood Center, Guangzhou, ChinaSearch for more papers by this authorYanli Ji, Corresponding Author Yanli Ji [email protected] Institute of Clinical Blood Transfusion, Guangzhou Blood Center, Guangzhou, China Correspondence Yanli Ji, 31 Luyuan Road, Yuexiu District, Guangzhou, 510095, China. Email: [email protected]Search for more papers by this author Chunyan Mo, Chunyan Mo orcid.org/0009-0003-4943-9524 Institute of Clinical Blood Transfusion, Guangzhou Blood Center, Guangzhou, ChinaSearch for more papers by this authorShuangshuang Jia, Shuangshuang Jia orcid.org/0000-0002-0092-8576 Institute of Clinical Blood Transfusion, Guangzhou Blood Center, Guangzhou, ChinaSearch for more papers by this authorGuangping Luo, Guangping Luo Institute of Clinical Blood Transfusion, Guangzhou Blood Center, Guangzhou, ChinaSearch for more papers by this authorYanli Ji, Corresponding Author Yanli Ji [email protected] Institute of Clinical Blood Transfusion, Guangzhou Blood Center, Guangzhou, China Correspondence Yanli Ji, 31 Luyuan Road, Yuexiu District, Guangzhou, 510095, China. Email: [email protected]Search for more papers by this author First published: 19 March 2024 https://doi.org/10.1111/trf.17795Read the full textAboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onEmailFacebookTwitterLinkedInRedditWechat No abstract is available for this article. CONFLICT OF INTEREST STATEMENT The authors have disclosed no conflicts of interest. REFERENCES 1Di Ciaccio P, Cutts B, Alahakoon TI, Dennington PM, Soo LA, Curnow J. Clinical consequences of the extremely rare anti-PP1Pk isoantibodies in pregnancy: a case series and review of the literature. Vox Sang. 2020; 116: 591–600. 10.1111/vox.13042 PubMedGoogle Scholar 2Westman JS, Stenfelt L, Vidovic K, Moller M, Hellberg A, Kjellstrom S, et al. Allele-selective RUNX1 binding regulates P1 blood group status by transcriptional control of A4GALT. Blood. 2018; 131: 1611–1616. 10.1182/blood-2017-08-803080 CASPubMedWeb of Science®Google Scholar 3Hellberg A, S-MA, Reid ME, Olsson ML. Expression of a novel missense mutation found in the A4GALT gene of Amish individuals with the pphenotype. Transfusion 2007; 48: 479–487. 10.1111/j.1537-2995.2007.01552.x PubMedGoogle Scholar 4Daniels G. Human blood groups. 3rd ed. Hoboken, NJ: Wiley-Blackwell; 2013. 10.1002/9781118493595 Google Scholar 5Wei L, Ji YL, Luo H, Mo CY, Zhang RQ, Zhao Y, et al. Serological and genetic study of a pedigree featuring a rare p phenotype [article in Chinese]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012; 29: 701–704. CASPubMedGoogle Scholar Early ViewOnline Version of Record before inclusion in an issue ReferencesRelatedInformation