Literature DB >> 3169800

Three Japanese families with members carrying C7 silent allele (C7*Q0). Possibility for an association between C7*Q0 and C6*B.

H Nishimukai1, H Kitamura, Y Takeuchi, T Shinomiya, Y Tamaki.   

Abstract

Three Japanese families with members carrying C7 silent allele(s) (C7*Q0) are presented. C6 types in the family members were also examined, and it was found that C7*Q0 was transmitted from a parent to offsprings as a haplotype, C7*Q0-C6*B. In another study of C6 types in sera from 3 volunteer blood donors with homozygous C7 deficiencies, the C6 phenotypes were found to be C6 B (homozygote). It seems remarkable that C7*Q0 can be associated with C6*B.

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Year:  1988        PMID: 3169800     DOI: 10.1159/000153792

Source DB:  PubMed          Journal:  Hum Hered        ISSN: 0001-5652            Impact factor:   0.444


  2 in total

1.  C7 M/N protein polymorphism typing applied to inherited deficiencies of human complement proteins C6 and C7.

Authors:  R Würzner; N Rance; P C Potter; M L Hendricks; P J Lachmann; A Orren
Journal:  Clin Exp Immunol       Date:  1992-09       Impact factor: 4.330

2.  DNA polymorphism of the human complement component C7 gene in familial deficiencies.

Authors:  E Coto; E Martínez-Naves; O Domínguez; C López-Larrea
Journal:  Hum Genet       Date:  1990-07       Impact factor: 4.132

  2 in total

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