{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,4]],"date-time":"2026-08-04T15:06:32Z","timestamp":1785855992171,"version":"3.56.0"},"reference-count":9,"publisher":"Wiley","issue":"3","license":[{"start":{"date-parts":[[2021,7,12]],"date-time":"2021-07-12T00:00:00Z","timestamp":1626048000000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by-nc-nd\/4.0\/"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["JPGN rep."],"published-print":{"date-parts":[[2021,8]]},"abstract":"<jats:sec><jats:label\/><jats:p><jats:italic>ARPC1B<\/jats:italic> is important in the maintenance and assembly of the ARP2\/3 complex. Loss of this complex due to <jats:italic>ARPC1B<\/jats:italic> mutation results in impairment of actin polymerization and subsequent defects in chemotaxis, cell migration, and DNA repair. Individuals with this rare mutation present in infancy and have abnormal innate and adaptive immune responses. They develop immune\u2010mediated inflammatory disease with associated platelet defects, eosinophilia, rashes, and bowel disease. Recurrent gastrointestinal hemorrhage has been described in known cases. Here, we report a case with endoscopic and histologic findings in a patient with this rare mutation.<\/jats:p><\/jats:sec>","DOI":"10.1097\/pg9.0000000000000095","type":"journal-article","created":{"date-parts":[[2021,7,12]],"date-time":"2021-07-12T15:00:19Z","timestamp":1626102019000},"source":"Crossref","is-referenced-by-count":5,"title":["<i>ARPC1B<\/i> Mutation Manifesting as Recurrent Hematemesis With Metaplasia"],"prefix":"10.1002","volume":"2","author":[{"given":"Swati","family":"Antala","sequence":"first","affiliation":[{"name":"Division of Gastroenterology, Hepatology and Nutrition Northwestern University, Feinberg School of Medicine Ann &amp; Robert H. 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