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We recently identified recessive mutations in the solute carrier organic anion transporter family member 2A1 gene ( SLCO2A1 ) as causative variants of chronic nonspecific multiple ulcers of the small intestine (chronic enteropathy associated with SLCO2A1 , CEAS). The aim of this study was to investigate the gastroduodenal expression of the SLCO2A1 protein in patients with CEAS and Crohn's disease (CD).

Distinction between Chronic Enteropathy Associated with the SLCO2A1 Gene and Crohn's Disease