Mitochondrial aspartate glutamate carrier (citrin) deficiency as the cause of adult-onset type II citrullinemia (CTLN2) and idiopathic neonatal hepatitis (NICCD)-Reference-Cited by-同舟云学术

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Mitochondrial aspartate glutamate carrier (citrin) deficiency as the cause of adult-onset type II citrullinemia (CTLN2) and idiopathic neonatal hepatitis (NICCD)

Published:2002-07 Issue:7 Volume:47 Page:333-341
ISSN:1434-5161
Container-title:Journal of Human Genetics
language:en
Short-container-title:J Hum Genet

Author:

Saheki T.,Kobayashi K.

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://www.nature.com/articles/jhg200253.pdf

Cited by 243 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. Citrin-deficient patient-derived induced pluripotent stem cells as a pathological liver model for congenital urea cycle disorders;Molecular Genetics and Metabolism Reports;2024-09

2. The therapeutic landscape of citrin deficiency;Journal of Inherited Metabolic Disease;2024-07-17

3. A rare case report: multiple intrahepatic masses in a pediatric patient with citrin deficiency;Discover Oncology;2024-05-31

4. Nutritional support therapy for liver transplantation in an adult-onset type II citrullinemia patient: a case report;Frontiers in Nutrition;2024-03-22

5. Rapid in vivo evaluation system for cholestasis-related genes in mice with humanized bile acid profiles;Hepatology Communications;2024-03-22

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