JOURNAL ARTICLE

Identification of a novel A allele with a nucleotide deletion c.198delG in the ABO gene associated with Ael phenotype.

  • Published In: Transfusion, 2024, v. 64, n. 4. P. E16 1 of 3

  • Database: Academic Search Ultimate 2 of 3

  • Authored By: Zheng, Haixiao; Peng, Chan; Wang, Min; Hong, Qinhan; Hua, Lin 3 of 3

Abstract

This article, published in the journal Transfusion, discusses the identification of a novel A allele with a nucleotide deletion c.198delG in the ABO gene associated with the Ael phenotype. The ABO blood group system, discovered by Karl Landsteiner over 100 years ago, plays a crucial role in blood transfusion and hemolysis disease of newborns. The study presents the case of a Chinese individual with the Ael phenotype and provides detailed methods and results of the ABO gene analysis. The authors conclude that this new allele with c.198delG is responsible for the Ael phenotype in the individual. [Extracted from the article]

Additional Information

  • Source:Transfusion. 2024/04, Vol. 64, Issue 4, pE16
  • Document Type:Article
  • Subject Area:Biography
  • Publication Date:2024
  • ISSN:0041-1132
  • DOI:10.1111/trf.17753
  • Accession Number:176496529
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