Genotypic and phenotypic features of citrin deficiency: Five-year experience in a Chinese pediatric center
Author:
Publisher
Spandidos Publications
Subject
Genetics,General Medicine
Cited by 70 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. Features of liver injury in 138 Chinese patients with NICCD;Journal of Pediatric Endocrinology and Metabolism;2023-11-10
3. Improved sensitivity and specificity for citrin deficiency using selected amino acids and acylcarnitines in the newborn screening;Journal of Inherited Metabolic Disease;2023-09-12
4. Citrin Deficiency: Clinical and Nutritional Features;Nutrients;2023-05-12
5. The prognosis of citrin deficiency differs between early-identified newborn and later-onset symptomatic infants;Pediatric Research;2023-04-07
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