Article
Typing of the nt343C>T (R95X) allele of the C9 gene by PCR-SSP and the allele frequency of R95X in five ethnic populations.
Legal medicine (Tokyo, Japan) - 1 Apr 2009
Tsujimura Ryusuke, Nishimukai Hiroaki, Okiura Tatsuyuki, Fukumori Yasuo, Tanabe Ryosuke, Orimoto Chitoshi, Ueda Norifumi
Abstract excerpt
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...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.
