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
2010 ◽
Vol 139
(5)
◽
pp. 1448-1450
◽
2008 ◽
Vol 86
(4)
◽
pp. 423-432
◽
2007 ◽
Vol 39
(12)
◽
pp. 1064-1070
◽
Keyword(s):
Keyword(s):