1. Mojtabavi, Helia, Fatehi, Farzad, Shahkarami, Sepideh, Rezaei, Nima, Nafissi, Shahriar. 2021. Novel Mutations of the TYMP Gene in Mitochondrial Neurogastrointestinal Encephalomyopathy: Case Series and Literature Review. In Journal of molecular neuroscience : MN, 71, 2526-2533. doi:10.1007/s12031-021-01822-w. https://pubmed.ncbi.nlm.nih.gov/33825174/
2. El-Hattab, Ayman W, Craigen, William J, Scaglia, Fernando. 2017. Mitochondrial DNA maintenance defects. In Biochimica et biophysica acta. Molecular basis of disease, 1863, 1539-1555. doi:10.1016/j.bbadis.2017.02.017. https://pubmed.ncbi.nlm.nih.gov/28215579/
3. Du, Jixiang, Zhang, Chao, Liu, Fuchen, Zhao, Yuying, Yan, Chuanzhu. 2023. Distinctive metabolic remodeling in TYMP deficiency beyond mitochondrial dysfunction. In Journal of molecular medicine (Berlin, Germany), 101, 1237-1253. doi:10.1007/s00109-023-02358-9. https://pubmed.ncbi.nlm.nih.gov/37603049/
4. Shah, Syed Asfand Yar, Shakeel, Hassan Abdullah, Hassan, Wajih Ul. 2022. Rare pathogenic mutation in the thymidine phosphorylase gene (TYMP) causing mitochondrial neurogastrointestinal encephalomyelopathy. In BMJ neurology open, 4, e000287. doi:10.1136/bmjno-2022-000287. https://pubmed.ncbi.nlm.nih.gov/36072350/
5. Venegas, Victor, Wang, Jing, Dimmock, David, Wong, Lee-Jun. . Real-time quantitative PCR analysis of mitochondrial DNA content. In Current protocols in human genetics, Chapter 19, Unit 19.7.. doi:10.1002/0471142905.hg1907s68. https://pubmed.ncbi.nlm.nih.gov/21234878/
6. El-Hattab, Ayman W, Scaglia, Fernando. . Mitochondrial DNA depletion syndromes: review and updates of genetic basis, manifestations, and therapeutic options. In Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics, 10, 186-98. doi:10.1007/s13311-013-0177-6. https://pubmed.ncbi.nlm.nih.gov/23385875/