Lipidomic analysis of human TANGO2-deficient cells suggests a lipid imbalance as a cause of TANGO2 deficiency disease
Author:
Funder
Canadian Institutes of Health Research
Publisher
Elsevier BV
Reference18 articles.
1. Functional genomics reveals genes involved in protein secretion and Golgi organization;Bard;Nature,2006
2. Mitochondrial dysfunction associated with TANGO2 deficiency;Heiman;Sci. Rep.,2022
3. The phenotype associated with variants in TANGO2 may be explained by a dual role of the protein in ER-to-Golgi transport and at the mitochondria;Milev;J. Inherit. Metab. Dis.,2021
4. Bi-Allelic Truncating mutations in TANGO2 cause infancy-onset recurrent metabolic crises with encephalocardiomyopathy;Kremer;Am. J. Hum. Genet.,2016
5. Recurrent muscle weakness with rhabdomyolysis, metabolic crises, and cardiac arrhythmia due to Bi-allelic TANGO2 mutations;Lalani;Am. J. Hum. Genet.,2016
Cited by 2 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. Cellular mechanisms of acute rhabdomyolysis in inherited metabolic diseases;Journal of Inherited Metabolic Disease;2024-08-12
2. TANGO2 deficiency disorder is predominantly caused by a lipid imbalance;Disease Models & Mechanisms;2024-06-01
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