Skip to main content

Heterogeneity in the genetic basis of human complement C9 deficiency

Immunogenetics volume 48, pages 144–147 (1998)Cite this article

This is a preview of subscription content, access via your institution.

Access options

Buy single article

Instant access to the full article PDF.

43,34 €

Price includes VAT (Finland)
Tax calculation will be finalised during checkout.

Author information

Affiliations

  1. Institute of Legal Medicine, Johannes Gutenberg University, Am Pulverturm 3, D-55131 Mainz, Germany, DE

    Konstanze Witzel-Schlömp, Christian Rittner, Thomas Kaufmann & P. M. Schneider

  2. Molecular Immunopathology Unit, Medical Research Council Centre, Cambridge, UK, GB

    Michael J. Hobart & Barbara A. Fernie

  3. Department of Microbiology, University College, Galway, Ireland, IE

    Ann Orren

  4. Institute of Hygiene, Leopold Franzens University, Innsbruck, Austria, AT

    Reinhard Würzner

Authors
  1. Konstanze Witzel-Schlömp
    View author publications

    You can also search for this author in PubMed Google Scholar

  2. Michael J. Hobart
    View author publications

    You can also search for this author in PubMed Google Scholar

  3. Barbara A. Fernie
    View author publications

    You can also search for this author in PubMed Google Scholar

  4. Ann Orren
    View author publications

    You can also search for this author in PubMed Google Scholar

  5. Reinhard Würzner
    View author publications

    You can also search for this author in PubMed Google Scholar

  6. Christian Rittner
    View author publications

    You can also search for this author in PubMed Google Scholar

  7. Thomas Kaufmann
    View author publications

    You can also search for this author in PubMed Google Scholar

  8. P. M. Schneider
    View author publications

    You can also search for this author in PubMed Google Scholar

Additional information

Received: 3 December 1997 / Revised: 4 February 1998

Rights and permissions

Reprints and Permissions

About this article

Cite this article

Witzel-Schlömp, K., Hobart, M., Fernie, B. et al. Heterogeneity in the genetic basis of human complement C9 deficiency. Immunogenetics 48, 144–147 (1998). https://doi.org/10.1007/s002510050415

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1007/s002510050415

  • Key words Point mutations
  • Hemolytic activity
  • Ethnic origin