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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
Experimental Biology and Medicine, ISSN 1535-3702, 6/2017, Volume 242, Issue 12, pp. 1271 - 1278
Journal Article
JOURNAL OF INHERITED METABOLIC DISEASE, ISSN 0141-8955, 05/2019, Volume 42, Issue 3, pp. 501 - 508
Journal Article
International Journal of Molecular Medicine, ISSN 1107-3756, 07/2011, Volume 28, Issue 1, pp. 33 - 40
Journal Article
Nature, ISSN 0028-0836, 11/2015, Volume 527, Issue 7578, pp. 379 - 383
Journal Article
International Journal of Clinical and Experimental Pathology, ISSN 1936-2625, 2017, Volume 10, Issue 3, pp. 3480 - 3487
Background: Neonatal intrahepatic cholestasis caused by citrin deficiency (NICCD) is an autosomal recessive metabolic disorder, which is caused by pathogenic... 
Neonatal intrahepatic cholestasis caused by citrin deficiency (NICCD), novel mutation | Next generation sequencing | Target sequence capture | SLC25A13 | target sequence capture | ONCOLOGY | novel mutation | MUTATION | neonatal intrahepatic cholestasis caused by citrin deficiency (NICCD) | PATHOLOGY
Journal Article
Biochimica et Biophysica Acta - Bioenergetics, ISSN 0005-2728, 11/2009, Volume 1787, Issue 11, pp. 1334 - 1341
Journal Article
世界胃肠病学杂志:英文版(电子版), ISSN 1007-9327, 2015, Issue 23, pp. 7331 - 7334
Citrin deficiency typically presents as neonatalintrahepatic cholestasis and resolves in late infancy.Here we report a case of citrin deficiency that... 
infection | deficiency | failure;Respiratory | Liver | Infant | Citrin | SLC25A13
Journal Article
Medical Journal of Wuhan University, ISSN 1671-8852, 03/2015, Volume 36, Issue 2, pp. 306 - 311
Journal Article
Internal Medicine, ISSN 0918-2918, 2019, Volume 58, Issue 13, pp. 1891 - 1895
Adult-onset type II citrullinemia (CTLN2) is a urea cycle disease characterized by neurological and psychiatric abnormalities associated with hyperammonemia.... 
NAFLD | fatty liver | hepatocyte steatosis | pathology | adult onset type II citrullinemia | CITRIN DEFICIENCY | MEDICINE, GENERAL & INTERNAL | HEPATITIS | GENE | SODIUM PYRUVATE | ASPARTATE GLUTAMATE CARRIER
Journal Article
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics, ISSN 1003-9406, 02/2019, Volume 36, Issue 2, pp. 116 - 119
Journal Article
Journal of the Korean Society of Neonatology, ISSN 1226-1513, 11/2011, Volume 18, Issue 2, pp. 370 - 373
Journal Article