Different regional distribution ofSLC25A13mutations in Chinese patients with neonatal intrahepatic cholestasis
Author:
Publisher
Baishideng Publishing Group Inc.
Subject
Gastroenterology,General Medicine
Cited by 25 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Clinical and genetic analysis of 26 Chinese patients with neonatal intrahepatic cholestasis due to citrin deficiency;Clinica Chimica Acta;2024-01
2. Update on the diagnosis and management of neonatal intrahepatic cholestasis caused by citrin deficiency: Expert review on behalf of the Asian Pan‐Pacific Society for Pediatric Gastroenterology, Hepatology, and Nutrition;Journal of Pediatric Gastroenterology and Nutrition;2023-12-10
3. Genetic and clinical features of patients with intrahepatic cholestasis caused by citrin deficiency;Journal of Pediatric Endocrinology and Metabolism;2023-05-08
4. Case report: Three novel variants on SLC25A13 in four infants with neonatal intrahepatic cholestasis caused by citrin deficiency;Frontiers in Pediatrics;2023-03-29
5. Pathogenic variants of the mitochondrial aspartate/glutamate carrier causing citrin deficiency;Trends in Endocrinology & Metabolism;2022-08
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