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pubmed-article:18620775pubmed:abstractTextCitrin deficiency caused by SLC25A13 gene mutations develops into adult-onset type II citrullinemia (CTLN2) and may be accompanied with hepatic steatosis and steatohepatitis. As its clinical features remain unclear, we aimed to explore the characteristics of fatty liver disease associated with citrin deficiency.lld:pubmed
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pubmed-article:18620775pubmed:articleTitleCitrin deficiency as a cause of chronic liver disorder mimicking non-alcoholic fatty liver disease.lld:pubmed
pubmed-article:18620775pubmed:affiliationDepartment of Gastroenterology, Shinshu University School of Medicine, Matsumoto, Japan.lld:pubmed
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