Article
Analysis of the molecular mechanism and pedigree investigation of para-Bombay phenotype caused by combined mutations at position h649 and h768 of FUT1 gene.
Blood transfusion = Trasfusione del sangue - 1 Sept 2022
Sun Xiaoye, Cai Yifeng, Ni Hui, Cao Xin, Ma Yudong, Zhang Yuan, Jiang Chen, Lu Jianxin, Cong Hui
Abstract excerpt
BACKGROUND: The para-Bombay phenotype is a rare red blood cell phenotype characterised by the lack of ABH antigens on red blood cells, but ABH substances can be found in saliva. The aim of this research was to study the mechanism of mutation of FUT1 and FUT2 genes and the pedigree of a family with the para-Bombay phenotype. MATERIAL AND METHODS: The blood group was detected by a conventional serological method, H...
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