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  1. No Access

    Chapter and Conference Paper

    Mutation Analysis in Hereditary Angioedema Identifies Patients at Risk for Develo** Acute and Life Threatening Edema

    Routine molecular genetic analysis identified the causative mutations in most of the HAE families. It is very important in diagnosing HAE carriers in affected families prior to clinical manifestation thus allo...

    T. Förster, A. Kocot, J. Schröder, W. Kreuz, E. Aygören-Pürsün… in 35th Hemophilia Symposium (2006)

  2. No Access

    Chapter and Conference Paper

    Mutation Analysis of the C1 Inhibitor Gene

    Frau Dipl. Biol. T. Förster, A. Kocot, Dr. J. Schröder… in 34th Hemophilia Symposium (2005)