Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: Hyperammonemia and SLC25A13[original query] |
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[Studies on the clinical manifestation and SLC25A13 gene mutation of Chinese patients with neonatal intrahepatic cholestasis caused by citrin deficiency]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2010 Apr 27 (2): 2. Xing Y, Qiu W, Ye J, Han L, Xu S, Zhang H, Gao X, Wang Y, Gu X |
SLC25A13 c.1610_1612delinsAT mutation in an Indian patient and literature review of 79 cases of citrin deficiency for genotype-phenotype associations. Gene 2018 5 668 190-195. Radha Rama Devi Akella, Naushad Shaik Mohamm |
Genetic background and clinical characteristics of infantile hyperammonemia. Translational pediatrics 2023 6 12 (5): 882-889. Mengyao Li, Xiang Chen, Huiyao Chen, Liyuan Hu, Yun Cao, Guoqiang Cheng, Laishuan Wang, Bingbing Wu, Wei Lu, Lin Yang, Wenhao Zh |
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