Literature DB >> 6663078

Polymorphism of the complement component C6 in Japanese.

K Tokunaga, Y Yukiyma, K Omoto.   

Abstract

Genetic polymorphism of human C6 was investigated in Japanese using isoelectric focusing and a specific haemolytic overlay method. Three common and six rare allotypes were identified. Five of these nine allotypes were reference-typed by the International Reference Laboratory. Five of the six rare allotypes were considered to be new. The allele frequencies were estimated in the population study as follows: C6 A 0.427, C6 B 0.483, C6 B2 0.076, and the rare alleles (A3, A21, M1, M2, B3, and B4) 0.014. Inheritance of the three common and the two rare (A3 and M1) allotypes was demonstrated in the family study. The patterns obtained by the pretreatment with neuraminidase are presented.

Entities:  

Mesh:

Substances:

Year:  1983        PMID: 6663078     DOI: 10.1111/j.1744-313x.1983.tb01029.x

Source DB:  PubMed          Journal:  J Immunogenet        ISSN: 0305-1811


  2 in total

1.  Family study on the polymorphisms of the sixth and seventh components (C6 and C7) of human complement: linkage and haplotype analyses.

Authors:  K Tokunaga; G Dewald; K Omoto; T Juji
Journal:  Am J Hum Genet       Date:  1986-09       Impact factor: 11.025

2.  C6 haplotypes: associations of a Dde I site polymorphism to complement deficiency genes and the Msp I restriction fragment length polymorphism (RFLP)

Authors:  B A Fernie; M J Hobart; G Delbridge; P C Potter; A Orren; P J Lachmann
Journal:  Clin Exp Immunol       Date:  1994-02       Impact factor: 4.330

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.