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

Art

J-GLOBAL ID：200902229867073280 Reference number：09A0538780

Typing of the nt343C>T (R95X) allele of the C9 gene by PCR-SSP and the allele frequency of R95X in five ethnic populations

PCR-SSPによるC9遺伝子のnt343C>T(R95X)アレルのタイピングおよび五つの民族集団でのR95Xのアレル頻度

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Material：
Volume： 11 Issue： Supplement 1 Page： S482-S483 Publication year： Apr. 2009
JST Material Number： W1412A ISSN： 1344-6223 Document type： Article
Article type：原著論文 Country of issue： Netherlands (NLD) Language： ENGLISH (EN)

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Genetics in general

Reference (7)：

INAI, S. Deficiency of the ninth component of the complement in man. J Clin Lab Immunol. 1979, 2, 85-87
FUKUMORI, Y. A high incidence of C9 deficiency among healthy blood donors in Osaka, Japan. Int Immunol. 1989, 1, 85-89
NAGATA, M. Inherited deficiency of ninth component of complement : an increased risk of meningococcal meningitis. J Pediatr. 1989, 114, 260-264
MARAZZITI, D. Relationships between the gene and protein structure in human complement component C9. Biochemistry. 1988, 27, 6529-6534
ABBOTT, C. The gene for human complement component C9 mapped to chromosome 5 by polymerase chain reaction. Genomics. 1989, 4, 606-609

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