Molecular genetic analysis of two novel ABO∗A alleles causing Ax phenotype in Chinese

Background: Mutations of ABO gene may cause the dysfunction of ABO glycosyltransferase (GT) that can result in weak ABO phenotypes. Here, we identified two novel weak ABO subgroup alleles and explored the mechanism that caused Ax phenotype. Materials and methods: The ABO phenotyping and genotyping w...

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Detalhes bibliográficos

Principais autores:	Hang Lei, Jiaming Li, Can Lou, Hui Zhang, Yuqing Shen, Naizhu Su, Xuefeng Wang, Xiaohong Cai, Yeling Lu
Formato:	Artigo
Idioma:	Inglês
Publicado em:	Elsevier 2025-09-01
coleção:	Journal of the Formosan Medical Association
Assuntos:	ABO Ax subgroup Mutation Novel allele
Acesso em linha:	http://www.sciencedirect.com/science/article/pii/S0929664624004066
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