MITOMAP References for RNA Mutation T2648C

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Index PMID Date Reference
1 32105570 2020 Aldosary, M., Al-Bakheet, A., Al-Dhalaan, H., Almass, R., Alsagob, M., Al-Younes, B., AlQuait, L., Mustafa, O. M., Bulbul, M., Rahbeeni, Z., Alfadhel, M., Chedrawi, A., Al-Hassnan, Z., AlDosari, M., Al-Zaidan, H., Al-Muhaizea, M. A., AlSayed, M. D., Salih, M. A., AlShammari, M., Faiyaz-Ul-Haque, M., Chishti, M. A., Al-Harazi, O., Al-Odaib, A., Kaya, N., Colak, D. (2020) Rett Syndrome, a neurodevelopmental disorder, whole-transcriptome, and mitochondrial genome multiomics analyses identify novel variations and disease pathways OMICS . 24 (3): 160-171 .