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adult-onset type ii citrullinemia (14) 14
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Clinical Transplantation, ISSN 0902-0063, 10/1997, Volume 11, Issue 5 I, pp. 453 - 458
Journal Article
Molecular Genetics and Metabolism Reports, ISSN 2214-4269, 2014, Volume 1, Issue 1, pp. 42 - 50
Citrin, encoded by , is a component of the malate-aspartate shuttle, which is the main NADH-transporting system in the liver. Citrin deficiency causes neonatal... 
Malate-aspartate shuttle | Neonatal intrahepatic cholestasis (NICCD) | Medium-chain triglycerides (MCT) | Adult-onset type II citrullinemia (CTLN2) | Citrin deficiency | SLC25A13
Journal Article
Internal Medicine, ISSN 0918-2918, 2005, Volume 44, Issue 3, pp. 188 - 195
Journal Article
Journal of Nutritional Science and Vitaminology, ISSN 0301-4800, 2011, Volume 57, Issue 3, pp. 239 - 245
Some patients with citrin deficiency caused by SLC25A13 gene mutations develop adult-onset type II citrullinemia (CTLN2) with hepatic encephalopathy. A recent... 
adult-onset type II citrullinemia (CTLN2) | PFC ratio | low-carbohydrate diet | Low-carbohydrate diet | Adult-onset type II citrullinemia (CTLN2) | SLC25A13 GENE | CITRIN DEFICIENCY | NUTRITION & DIETETICS | THERAPY | CTLN2 | MUTATIONS | IDENTIFICATION | ASPARTATE-GLUTAMATE CARRIER
Journal Article
Journal of the Korean Society of Neonatology, ISSN 1226-1513, 11/2010, Volume 17, Issue 2, pp. 250 - 253
Journal Article
Application of Clinical Genetics, ISSN 1178-704X, 2018, Volume 11, pp. 163 - 170
Journal Article
Epilepsia, ISSN 0013-9580, 12/2010, Volume 51, Issue 12, pp. 2484 - 2487
Journal Article