MTRF1L

Soleimanpour-Lichaei, H. R.؛ Kühl, I.؛ Gaisne, M.؛ Passos, J. F.؛ Wydro, M.؛ Rorbach, J.؛ Temperley, R.؛ Bonnefoy, N.؛ Tate, W.؛ Lightowlers, R.؛ Chrzanowska-Lightowlers, Z. (2007)، "MtRF1a is a Human Mitochondrial Translation Release Factor Decoding the Major Termination Codons UAA and UAG"، Molecular Cell، 27 (5): 745–757، doi:10.1016/j.molcel.2007.06.031، PMC 1976341، PMID 17803939. Nozaki, Y.؛ Matsunaga, N.؛ Ishizawa, T.؛ Ueda, T.؛ Takeuchi, N. (2008)، "HMRF1L is a human mitochondrial translation release factor involved in the decoding of the termination codons UAA and UAG"، Genes to Cells، 13 (5): 429–438، doi:10.1111/j.1365-2443.2008.01181.x، PMID 18429816. Ishizawa, T.؛ Nozaki, Y.؛ Ueda, T.؛ Takeuchi, N. (2008)، "The human mitochondrial translation release factor HMRF1L is methylated in the GGQ motif by the methyltransferase HMPrmC"، Biochemical and Biophysical Research Communications، 373 (1): 99–103، doi:10.1016/j.bbrc.2008.05.176، PMID 18541145. Vieira, A. R.؛ McHenry, T. G.؛ Daack-Hirsch, S.؛ Murray, J. C.؛ Marazita, M. L. (2008)، "Candidate Gene/Loci Studies in Cleft Lip/Palate and Dental Anomalies Finds Novel Susceptibility Genes for Clefts"، Genetics in Medicine، 10 (9): 668–674، doi:10.1097/GIM.0b013e3181833793، PMC 2734954، PMID 18978678. Antonicka, H.؛ Østergaard, E.؛ Sasarman, F.؛ Weraarpachai, W.؛ Wibrand, F.؛ Pedersen, A. M. B.؛ Rodenburg, R. J.؛ Van Der Knaap, M. S.؛ Smeitink, J. A. M.؛ Chrzanowska-Lightowlers, Z. M.؛ Shoubridge, E. A. (2010)، "Mutations in C12orf65 in Patients with Encephalomyopathy and a Mitochondrial Translation Defect"، The American Journal of Human Genetics، 87 (1): 115–122، doi:10.1016/j.ajhg.2010.06.004، PMC 2896764، PMID 20598281.