A novel mutation W388X underlying properdin deficiency in a Finnish family

Benzer Materyaller

• Lack of Complement Inhibitors in the Outer Intracranial Artery Aneurysm Wall Associates with Complement Terminal Pathway Activation
  Yazar:: Tulamo, Riikka, ve diğerleri
  Baskı/Yayın Bilgisi: (2010)
• Y402H Polymorphism of Complement Factor H Affects Binding Affinity to C-Reactive Protein()
  Yazar:: Laine, Matti, ve diğerleri
  Baskı/Yayın Bilgisi: (2007)
• Binding of C-reactive protein to modified low-density-lipoprotein particles: identification of cholesterol as a novel ligand for C-reactive protein.
  Yazar:: Taskinen, Sanna, ve diğerleri
  Baskı/Yayın Bilgisi: (2002)
• Streptococcus pneumoniae Capsular Serotype 19F Is More Resistant to C3 Deposition and Less Sensitive to Opsonophagocytosis than Serotype 6B
  Yazar:: Melin, Merit, ve diğerleri
  Baskı/Yayın Bilgisi: (2009)
• Carrier detection in families with properdin deficiency by microsatellite haplotyping.
  Yazar:: Kölble, K, ve diğerleri
  Baskı/Yayın Bilgisi: (1993)