P220 - The NOD2 variants rs2066843 and rs2076756 are novel independent Crohn's disease susceptibility gene variants associated with severe penetrating disease phenotype resulting in frequent need for surgery

✍ Scribed by J. Seiderer; J. Glas; J. Diegelmann; G. Pasciuto; C. Tillack; S. Pfennig; M. Jürgens; A. Konrad; H. Török; U. Schiemann; T. Griga; W. Klein; J.T. Epplen; T. Mussack; P. Lohse; B. Göke; T. Ochsenkühn; M. Folwaczny; B. Müller-Myhsok; S. Brand

• Book ID: 119636335
• Publisher: Oxford University Press
• Year: 2009
• Tongue: English
• Weight: 47 KB
• Volume: 3
• Category: Article
• ISSN: 1873-9946
• DOI: 10.1016/s1873-9946(09)60247-6