A Rare Cause of Blood in Stool and Anemia
Author:
Funder
Medical Science and Technology Project of Zhejiang Province
Health Commission of Zhejiang Province
Chinese Medicine Research Program of Zhejiang Province
Publisher
Elsevier BV
Reference9 articles.
1. A hereditary enteropathy caused by mutations in the SLCO2A1 gene, encoding a prostaglandin transporter;Umeno;PLoS Genet,2015
2. Pathogenesis of chronic enteropathy associated with the SLCO2A1 gene: hypotheses and conundrums;Xie;World J Gastroenterol,2024
3. Interplay between the prostaglandin transporter OATP2A1 and prostaglandin E2-mediated cellular effects;Bujok;Cell Signal,2015
4. Clinical and genetic characteristics of Chinese patients diagnosed with chronic enteropathy associated with SLCO2A1 gene;Shang;Orphanet J Rare Dis,2024
5. Clinical and genetic characteristics of Korean patients diagnosed with chronic enteropathy associated with SLCO2A1 gene: a KASID multicenter study;Hong;Gut Liver,2022
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