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Typing of the nt343C>T (R95X) allele of the C9 gene by PCR-SSP and the allele frequency of R95X in five ethnic populations.
Tsujimura, Ryusuke; Nishimukai, Hiroaki; Okiura, Tatsuyuki; Fukumori, Yasuo; Tanabe, Ryosuke; Orimoto, Chitoshi; Ueda, Norifumi.
Afiliação
  • Tsujimura R; Department of Legal Medicine, Ehime University Graduate School of Medicine, Ehime 791-0295, Japan.
Leg Med (Tokyo) ; 11 Suppl 1: S482-3, 2009 Apr.
Article em En | MEDLINE | ID: mdl-19261509
One of the alleles which leads to ninth component of complement deficiency (C9D) is R95X (nt343C>T), which is present in most cases of C9D in Japan. In this study, we carried out nt343C>T typing by the method of polymerase chain reaction with sequence-specific primers (PCR-SSP), and showed the frequency of the R95X allele in German, Italian, Thai, Korean and Chinese populations. We did not find the R95X allele in the German or Italian populations. The allele frequency of R95X in the three Asian populations is as follows: Thais 0.019, Koreans 0.008, and Chinese 0.002. As the allele frequency in the Japanese population is 0.036, the results provide supporting evidence that the R95X is an allele characteristic of Japanese.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Etnicidade / Impressões Digitais de DNA / Frequência do Gene Limite: Humans Idioma: En Revista: Leg Med (Tokyo) Assunto da revista: JURISPRUDENCIA Ano de publicação: 2009 Tipo de documento: Article País de afiliação: Japão

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Etnicidade / Impressões Digitais de DNA / Frequência do Gene Limite: Humans Idioma: En Revista: Leg Med (Tokyo) Assunto da revista: JURISPRUDENCIA Ano de publicação: 2009 Tipo de documento: Article País de afiliação: Japão