ABO*B.01+c.464A>C represents a missense variation in the ABO gene and encodes a weak B phenotype-Reference-Cited by-同舟云学术

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ABO*B.01+c.464A>C represents a missense variation in the ABO gene and encodes a weak B phenotype

Published:2021-07-29 Issue:9 Volume:61 Page:
ISSN:0041-1132
Container-title:Transfusion
language:en
Short-container-title:Transfusion

Author:

Feng Chenchen¹^ORCID,Li Hui²,Liu Taixiang¹,Xiao Jianyu¹,Huang Chengyin¹,Flegel Willy A.³⁴^ORCID,Chen Qing¹⁵^ORCID

Affiliation:

1. Transfusion Research Department Jiangsu Province Blood Center Nanjing China

2. School of Public Health Nanjing Medical University Nanjing China

3. Department of Transfusion Medicine, NIH Clinical Center National Institutes of Health Bethesda Maryland USA

4. Huazhong University of Science and Technology Wuhan China

5. Center for Global Health, School of Public Health Nanjing Medical University Nanjing China

Publisher

Wiley

Subject

Hematology,Immunology,Immunology and Allergy

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/trf.16597

Reference5 articles.

1. A new missense mutation c.692C>A caused a weak Ael phenotype in a Chinese individual

2. Genomic analysis of blood samples with serologicABOdiscrepancy identifies 12 novel alleles in a Chinese Han population

3. A novel B allele with c.502C>G mutation identified in a Chinese individual

4. A NovelABOGene Variant Leads to Discrepant Results in Forward/Reverse and Molecular Blood Grouping

5. A novel B allele with c.28 + 5885C>T substitution in the erythroid cell-specific regulatory element identified in an individual with phenotype B3

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