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Gene, ISSN 0378-1119, 04/2019, Volume 693, pp. 69 - 75
The human gene encodes the liver type aspartate/glutamate carrier isoform 2 (AGC2, commonly named as citrin), which plays a key role in the main NADH-shuttle... 
Promoter | SLC25A13 gene | Mutation | Dual-luciferase reporter assay | Citrin deficiency | CITRIN DEFICIENCY NICCD | NF-Y | EAST-ASIA | IDENTIFICATION | FEATURES | NEONATAL INTRAHEPATIC CHOLESTASIS | GENETICS & HEREDITY | II CITRULLINEMIA | ASPARTATE GLUTAMATE CARRIER | MUTATIONS | BINDING | Anopheles | Codon | Analysis | Genes | Luciferase | Genetic research | Genetic transcription | Genetic translation | Index Medicus
Journal Article
Nature Genetics, ISSN 1061-4036, 06/1999, Volume 22, Issue 2, pp. 159 - 163
Journal Article
Molecular Genetics and Metabolism, ISSN 1096-7192, 2011, Volume 103, Issue 3, pp. 293 - 296
Mutations of the gene, which encodes citrin, result in adult-onset type II citrullinemia (CTLN2). Because CTLN2 has been associated with hepatocellular... 
Hepatocellular carcinoma | Adult-onset type II citrullinemia | SLC25A13 mutation | Liver cancer | Carcinoma | Gene mutations | Analysis | Genetic research | Disease susceptibility | Genetic aspects | Cancer | DNA | Point mutation | genomics | Hepatitis B | Tumors
Journal Article
Chinese Journal of Medical Genetics, ISSN 1003-9406, 10/2017, Volume 34, Issue 5, pp. 676 - 679
Journal Article
Journal Article
Journal of Pediatric Endocrinology and Metabolism, ISSN 0334-018X, 03/2015, Volume 28, Issue 3, pp. 471 - 475
Journal Article
Journal of Human Genetics, ISSN 1434-5161, 6/2008, Volume 53, Issue 6, pp. 534 - 545
Journal Article
Journal of Human Genetics, ISSN 1434-5161, 7/2005, Volume 50, Issue 7, pp. 338 - 346
Journal Article
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