Literature DB >> 10072634

Terminal complement component deficiencies in Japan.

Y Fukumori1, T Horiuchi.   

Abstract

From the serological screening for complement component deficiencies, we found 2 subjects with inherited C5 deficiency (C5D), 4 with C6D, 6 with C7D, 4 with C81 (alpha-gamma subunit) D and 138 with C9D among 145,640 healthy Japanese blood donors. Recently, the genetic bases of some of the C6D, C7D, C81D and C9D Japanese individuals were elucidated using an exon-specific PCR-SSCP method followed by direct sequencing of the target exons.

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Year:  1998        PMID: 10072634     DOI: 10.1159/000019078

Source DB:  PubMed          Journal:  Exp Clin Immunogenet        ISSN: 0254-9670


  2 in total

Review 1.  Complement deficiency.

Authors:  K M O'Neil
Journal:  Clin Rev Allergy Immunol       Date:  2000-10       Impact factor: 8.667

2.  A Point Mutation Creating a 3' Splice Site in C8A Is a Predominant Cause of C8α-γ Deficiency in African Americans.

Authors:  Peter Densen; Laynez Ackermann; Leslie Saucedo; Julio E Figueroa; Zhi-Hai Si; Conrad Martin Stoltzfus
Journal:  J Immunol       Date:  2020-08-07       Impact factor: 5.422

  2 in total

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