1. WHOLE EXOME SEQUENCING OF A MULTIPLEX CROHN'S DISEASE FAMILY IDENTIFIES RARE ALTERATIONS IN PYGB ANDXRN2 AS POTENTIALLY HIGH IMPACT RISK VARIANTS OF DISEASE. (26th January 2023) Authors: Chen, Lea Ann; Kim, Minsuk; Li, Dalin; Aita, Rohit; Cataldo, Susan; Radin, Arielle; Baylor, Jessica; Deng, Lily; Hahn, Brett; Wong, Kevin; Tin, Kevin; Mengesha, Emebet; McGovern, Dermot Journal: Inflammatory bowel diseases Issue: Volume 29(2023)Supplement 1 Page Start: S40 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗