Hereditary complement C7 deficiency in nine families: Subtotal C7 deficiency revisited

Deficiencies in terminal complement components, including the component C7, are uncommon and associated with an increased risk of recurrent systemic neisserial infection. A total of 22 molecular defects have been reported in the C7 gene with both complete (C7Q0) and subtotal (C7SD) C7 deficiencies....

Ausführliche Beschreibung

Gespeichert in:

Bibliographische Detailangaben
Veröffentlicht in:	European Journal of Immunology 2007-05, Vol.37 (5), p.1377-1385
Hauptverfasser:	Rameix‐Welti, Marie‐Anne, Régnier, Catherine H., Bienaimé, Frank, Blouin, Jacques, Schifferli, Jurg, Fridman, Wolf H., Sautès‐Fridman, Catherine, Frémeaux‐Bacchi, Veronique
Format:	Artikel
Sprache:	eng
Schlagworte:	Adolescent Adult Blood Protein Disorders - genetics Child, Preschool Complement Complement C7 - deficiency Complement C7 - genetics Female Fluorescent Antibody Technique Human Humans Immune System Diseases - genetics Immunodeficiency disease Male Meningococcal Infections - genetics Meningococcal Infections - immunology Molecular biology Mutation Neisseria meningitidis Pedigree Reverse Transcriptase Polymerase Chain Reaction Transfection
Online-Zugang:	Volltext
Tags:	Tag hinzufügen Keine Tags, Fügen Sie den ersten Tag hinzu!

Schreiben Sie den ersten Kommentar!