Factor H mutations in SCR1–4 and SCR6–9 are equally important genetic susceptibility factors for atypical Haemolytic Uraemic Syndrome as the mutations in SCR19–20

✍ Scribed by Lubka Roumenina; Marie Frimat; Fadi Fakhouri; Chantal Loirat; Sylvain Bigot; Catherine Sautes-Fridman; Lise Halbwachs-Mecarelli; Véronique Frémeaux-Bacchi

• Book ID: 116757482
• Publisher: Elsevier Science
• Year: 2009
• Tongue: English
• Weight: 67 KB
• Volume: 46
• Category: Article
• ISSN: 0161-5890
• DOI: 10.1016/j.molimm.2009.05.313