Two novel mutations p. L319V and p. L91P in ABO glycosyltransferases lead to A(el) and B(el) phenotypes

BACKGROUND: Mutations of the 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 their mechanisms that caused A(el) and B(el) phenotypes. MATERIALS AND METHODS: The ABO phenoty...

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Bibliografische gegevens
Gepubliceerd in:Blood Transfus
Hoofdauteurs: Lei, Hang, Wang, Zhongying, Wang, Yuqing, Xiang, Dong, Wang, Xuefeng, Cai, Xiaohong
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: Edizioni SIMTI - SIMTI Servizi Srl 2020
Onderwerpen:
Immunohaematology
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC7605879/
https://ncbi.nlm.nih.gov/pubmed/32281923
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2450/2020.008-20
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