Adult‐onset type <scp>II citrullinemia</scp> manifested as hepatosteatosis or steatohepatitis: A report of three <scp>Chinese</scp> cases-Reference-Cited by-同舟云学术

Adult‐onset type II citrullinemia manifested as hepatosteatosis or steatohepatitis: A report of three Chinese cases

Published:2022-04 Issue:4 Volume:23 Page:240-245
ISSN:1751-2972
Container-title:Journal of Digestive Diseases
language:en
Short-container-title:J of Digest Diseases

Author:

Wang Min¹^ORCID,Zhao Xin Yan¹,Wang Yu¹,Wang Xiao Ming¹,Yazaki Masahide²,Saheki Takeyori³,Jia Ji Dong¹,Zhang Chun Hua⁴,Ou Xiao Juan¹,Wang Tai Ling⁵

Affiliation:

1. Liver Research Center, Beijing Friendship Hospital Capital Medical University, Beijing Key Laboratory of Translational Medicine in Liver Cirrhosis & National Clinical Research Center of Digestive Diseases Beijing China

2. Institute for Biomedical Sciences Shinshu University Matsumoto Japan

3. Department of Hygiene and Health Promotion Medicine Kagoshima University Graduate School for Medical and Dental Sciences Kagoshima Japan

4. Department of Research & Development MILS International Yokohama Japan

5. Department of Pathology China‐Japan Friendship Hospital Beijing China

Funder

Digestive Medical Coordinated Development Center of Beijing Hospitals Authority

Publisher

Wiley

Subject

Gastroenterology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/1751-2980.13096

Reference25 articles.

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

2. Genotypic and phenotypic features of citrin deficiency: five‐year experience in a Chinese pediatric center;Song YZ;Int J Mol Med.,2011

3. SLC25A13 Gene Analysis in Citrin Deficiency: Sixteen Novel Mutations in East Asian Patients, and the Mutation Distribution in a Large Pediatric Cohort in China

4. Molecular diagnosis of pediatric patients with citrin deficiency in China: SLC25A13 mutation spectrum and the geographic distribution

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