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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.
Artículo en Chino | 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.
Asunto(s)
Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Sistema del Grupo Sanguíneo Rh-Hr / Intrones / China / Exones / Pueblo Asiatico / Alelos / Genética / Genotipo Tipo de estudio: Estudio pronóstico Límite: Humanos País/Región como asunto: Asia Idioma: Chino Revista: Chinese Journal of Medical Genetics Año: 2019 Tipo del documento: Artículo

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Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Sistema del Grupo Sanguíneo Rh-Hr / Intrones / China / Exones / Pueblo Asiatico / Alelos / Genética / Genotipo Tipo de estudio: Estudio pronóstico Límite: Humanos País/Región como asunto: Asia Idioma: Chino Revista: Chinese Journal of Medical Genetics Año: 2019 Tipo del documento: Artículo