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ACG Clinical Guideline: Gastroparesis

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doi: 10.1016/s0163-7258(02)00297-8

Wilson's disease, an autosomal recessive disorder caused by mutations in the ATP7B gene leading to copper accumulation, and alpha-1 antitrypsin (A1AT) deficiency, linked to mutations in the SERPINA1 gene, are significant contributors to hepatic steatosis [3,9]

Below are examples of GLP-1 agonists commonly prescribed for diabetes or weight loss

All statistical analyses were performed with SAS software, version 9.4 TS1M5 (SAS Institute)
