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A case with a novel weak D type / 中华医学遗传学杂志
Chinese Journal of Medical Genetics ; (6): 731-733, 2019.
Article in Chinese | WPRIM | ID: wpr-776818
ABSTRACT
OBJECTIVE@#To report on a novel weak D type identified in a Chinese individual.@*METHODS@#Peripheral blood sample was collected for a voluntary blood donor with weakened expression of D antigen. Routine serological testing was carried out to determine the D, C, c, E and e antigens of the Rh blood group. A D-screening kit was used to analyze the RhD epitopes. The 10 exons and flanking intronic regions of the RHD gene were sequenced. The zygosity of RHD was determined with a sequence-specific primer PCR method.@*RESULTS@#A novel RHD allele, RHD (1022T>A), was found in the subject with a weak D phenotype. Serological testing of the RhD epitopes has coined with the weak D phenotype.@*CONCLUSION@#A novel weak D allele has been identified in Chinese population.
Subject(s)
Full text: Available Index: WPRIM (Western Pacific) Main subject: Rh-Hr Blood-Group System / Introns / China / Exons / Asian People / Alleles / Genetics / Genotype Type of study: Prognostic study Limits: Humans Country/Region as subject: Asia Language: Chinese Journal: Chinese Journal of Medical Genetics Year: 2019 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Rh-Hr Blood-Group System / Introns / China / Exons / Asian People / Alleles / Genetics / Genotype Type of study: Prognostic study Limits: Humans Country/Region as subject: Asia Language: Chinese Journal: Chinese Journal of Medical Genetics Year: 2019 Type: Article