A novelcis-ABvariant allele arising from ade novonucleotide substitution c.796A>G (p.M266V) in the B glycosyltransferase gene

Author:

Lee S. Y.1,Phan M. T. T.12,Shin D. J.13,Shin M. G.1,Park J. T.4,Shin J. W.5,Yazer M. H.67,Shin H. B.8,Cho D.9

Affiliation:

1. Department of Laboratory Medicine; Chonnam National University Medical School; Gwangju Korea

2. Center for Creative Biomedical Scientists; Chonnam National University; Gwangju Korea

3. Department of Companion & Laboratory Animal Science; Kongju National University; Yesan Korea

4. Department of Forensic Medicine; Chonnam National University Medical School; Gwangju Korea

5. Department of Laboratory Medicine; Soonchunhyang University Hospital; Seoul Korea

6. Department of Pathology; University of Pittsburgh; Pittsburgh Pennsylvania USA

7. Institute for Transfusion Medicine; University of Pittsburgh; Pittsburgh Pennsylvania USA

8. Department of Laboratory Medicine and Genetics; Soonchunhyang University College of Medicine; Bucheon Korea

9. Department of Laboratory Medicine and Genetics; Samsung Medical Center, Sungkyunkwan University School of Medicine; Seoul Korea

Funder

Soonchunhyang University Research Fund

Publisher

Wiley

Subject

Hematology

Reference14 articles.

1. Use of cell study models to confirm the weak ABO phenotypes caused by point mutations among Taiwanese;Chen;Annals of Clinical Laboratory Science,2011

2. The serological and genetic basis of the cis-AB blood group in Korea;Cho;Vox Sanguinis,2004a

3. A novel B(var) allele (547 G>A) demonstrates differential expression depending on the co-inherited ABO allele;Cho;Vox Sanguinis,2004b

4. Chimerism and mosaicism are important causes of ABO phenotype and genotype discrepancies;Cho;Immunohematology,2006

5. The M142T mutation causes B3 phenotype: three cases and an in vitro expression study;Cho;The Korean Journal of Laboratory Medicine,2010

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