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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Vydáno v:Blood Transfus
Hlavní autoři: Lei, Hang, Wang, Zhongying, Wang, Yuqing, Xiang, Dong, Wang, Xuefeng, Cai, Xiaohong
Médium: Artigo
Jazyk:Inglês
Vydáno: Edizioni SIMTI - SIMTI Servizi Srl 2020
Témata:
Immunohaematology
On-line přístup: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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