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Genetic Risk Variants for Celiac Disease in the IL2/IL21 Locus are Associated with Eosinophilic Esophagitis

✍ Scribed by Sherrill, J.; Martin, L.; Blanchard, C.; Annaiah, K.; Spergel, J.; Hakonarson, H.; Rothenberg, M.


Book ID
119283300
Publisher
Elsevier Science
Year
2010
Tongue
English
Weight
41 KB
Volume
125
Category
Article
ISSN
1097-6825

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## Communicated by Pui-Yan Kwok Risk for late onset Alzheimer disease (LOAD) and plasma amyloid beta levels (Ab42; encoded by APP), an intermediate phenotype for LOAD, show linkage to chromosome 10q. Several strong candidate genes (VR22, PLAU, IDE) lie within the 1-lod support interval for linkage