Literature DB >> 10838521

D(Va) category phenotype and genotype in Japanese families.

T J Legler1, V Wiemann, H Ohto, I Matuda, T Obara, M Uchikawa, M Köhler.   

Abstract

BACKGROUND AND OBJECTIVES: The genetic background of the D(Va) category phenotype has been described in two Caucasian individuals. We were interested in the RHD sequence of 7 Japanese D(Va) individuals and their families.
MATERIALS AND METHODS: With SSP-PCR we tested exons 4, 5 and 7 of the RHD gene and used restriction enzymes for testing nucleotide associated with the D(Va) phenotype.
RESULTS: A single RHD G667 C697 allele was present in 5 individuals with D(Va) category phenotype, and in 2 individuals we found a D-CE-D hybrid gene (exon 5 had been replaced). The D(Va)Ce gene complex was found in all families.
CONCLUSION: The changes of the RHD gene described in European D(Va) individuals were also observed in Japanese families.

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Year:  2000        PMID: 10838521     DOI: 10.1159/000031179

Source DB:  PubMed          Journal:  Vox Sang        ISSN: 0042-9007            Impact factor:   2.144


  1 in total

1.  Whole exon 5 and intron 5 replaced by RHCE in DVa(Hus).

Authors:  Chaopeng Shao; Wen Xiong; Wei Wang
Journal:  J Hum Genet       Date:  2004-01-09       Impact factor: 3.172

  1 in total

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