The development of anin vitrocerebral organoid model for investigating the pathomolecular mechanisms associated with the central nervous system involvement in Mitochondrial Neurogastrointestinal Encephalomyopathy (MNGIE)
Author:
Affiliation:
1. Molecular & Clinical Sciences Research Institute, St. George’s, University of London, United Kingdom
Publisher
Informa UK Limited
Subject
Genetics,Molecular Medicine,Biochemistry,General Medicine
Link
https://www.tandfonline.com/doi/pdf/10.1080/15257770.2018.1492139
Reference30 articles.
1. Mitochondrial neurogastrointestinal encephalomyopathy: An autosomal recessive disorder due to thymidine phosphorylase mutations
2. Mitochondrial Neurogastrointestinal Encephalomyopathy (MNGIE): A Disease of Two Genomes
3. Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE)
4. Elevated plasma deoxyuridine in patients with thymidine phosphorylase deficiency
5. Site-specific somatic mitochondrial DNA point mutations in patients with thymidine phosphorylase deficiency
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