Sequence variants in the proximal promoter and +5.8‐kb site of ABO in Koreans with weak B phenotypes-Reference-Cited by-同舟云学术

Sequence variants in the proximal promoter and +5.8‐kb site of ABO in Koreans with weak B phenotypes

Published:2021-09-28 Issue: Volume: Page:
ISSN:0042-9007
Container-title:Vox Sanguinis
language:en
Short-container-title:Vox Sanguinis

Author:

Yu HongBi¹^ORCID,Kim Tae Yeul²^ORCID,Moon Sue Jin¹,Chung Yoo Na³,Yoo Hwa Jong²,Kim Jeong Hoon¹,Cho Duck¹²^ORCID

Affiliation:

1. Department of Health Sciences and Technology, Samsung Advanced Institute for Health Sciences and Technology Sungkyunkwan University Seoul South Korea

2. Department of Laboratory Medicine and Genetics, Samsung Medical Centre Sungkyunkwan University School of Medicine Seoul South Korea

3. Department of Laboratory Medicine Dankook University Hospital Cheonan South Korea

Publisher

Wiley

Subject

Hematology,General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/vox.13207

Reference20 articles.

1. Molecular genetic analysis of ABO blood group variations reveals 29 novel ABO subgroup alleles

2. Genomic analysis of clinical samples with serologic ABO blood grouping discrepancies: identification of 15 novel A and B subgroup alleles

3. Weak blood group B phenotypes may be caused by variations in the CCAAT-binding factor/NF-Y enhancer region of the ABO gene

4. Expression of ABO blood-group genes is dependent upon an erythroid cell–specific regulatory element that is deleted in persons with the Bm phenotype

5. Mutation of the GATA site in the erythroid cell-specific regulatory element of the ABO gene in a Bmsubgroup individual

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