المؤلفون: Hathazi, D., Griffin, H., Jennings, M. J., Giunta, M., Powell, C., Pearce, S. F., Munro, B., Wei, W., Boczonadi, V., Poulton, J., Pyle, A., Calabrese, C., Gomez-Duran, A., Schara, U., Pitceathly, R. D., Hanna, M. G., Joost, K., Cotta, A., Paim, J. F., Navarro, M. M., Duff, J., Mattmann, A., Chapman, K., Servidei, S., Della Marina, A., Uusimaa, J., Roos, A., Mootha, V., Hirano, M., Tulinius, Mar, 1953, Giri, M., Hoffmann, E. P., Lochmuller, H., DiMauro, S., Minczuk, M., Chinnery, P. F., Muller, J. S., Horvath, R.

المصدر: Embo Journal. 39(23)

مصطلحات موضوعية: Pediatrics, Pediatrik, Clinical Medicine, Klinisk medicin, digenic inheritance, homoplasmic tRNA mutation, mitochondrial myopathy, reversible infantile respiratory chain deficiency, citric-acid cycle, stress-response, mitochondrial translation, reaction-mechanism, fatty-acid, key role, rna, glutaminase, regulator, oxidation, Biochemistry & Molecular Biology, Cell Biology

URL الوصول: https://gup.ub.gu.se/publication/298047