Genetic Association Analysis Reveals Differences in the Contribution of NOD2 Variants to the Clinical Phenotypes of Orofacial Granulomatosis - Concepedia

Concepedia

Publication | Open Access

Genetic Association Analysis Reveals Differences in the Contribution of NOD2 Variants to the Clinical Phenotypes of Orofacial Granulomatosis

DOI Full Paper Access

16

Citations

43

References

2016

Year

Alexander J. Mentzer, Shalini Nayee, Yasmin Omar, Esther Hullah, Kirstin M. Taylor, Rishi Goel, Hannah Bye, Tarik Shembesh, Timothy R. Elliott, Helen Campbell,

Inflammatory Bowel Diseases

Abstract

Our findings suggest that genetic variants in NOD2 are only associated with OFG in patients with concurrent intestinal disease. A genome-wide association scan is needed to fully define the genetic architecture of OFG.

References

	Year	Citations

Page 1