Identification of the RHD novel allele c. 801+2T>G and study of its effect on RhD phenotype in vitro

Identification of the RHD novel allele c. 801+2T>G and study of its effect on RhD phenotype in vitro

[Objective] To further identify the RhD phenotype and RHD genotype in the individual who have RhD negative phenotype in the primary screening, and to analyze the effect of c. 801+2T>G mutation on RhD phenotype by minigene splicing assay. [Methods] The serologic test was performed for RhD phenotyp...

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Bibliographic Details
Main Authors: JIA Shuangshuang, WEN Jizhi, WEI Ling, ZHANG Runqing, LUO Guangping, JI Yanli
Format: Article
Language:zho
Published: Institute of Blood Transfusion of Chinese Academy of Medical Sciences 2024-12-01
Series:Zhongguo shuxue zazhi
Subjects:
rhd phenotype
rhd novel allele
c. 801+2t>g mutation
minigene splicing assay
Online Access:https://www.cjbt.cn/thesisDetails#10.13303/j.cjbt.issn.1004-549x.2024.12.015&lang=en
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