Citations for
1COXPD15, MTFMT
Clinical and functional characterisation of the combined respiratory chain defect in two sisters due to autosomal recessive mutations in MTFMT.
Neeve VC, Pyle A, Boczonadi V, Gomez-Duran A, Griffin H, Santibanez-Koref M, Gaiser U, Bauer P, Tzschach A, Chinnery PF, Horvath R.
Mitochondrion itochondrion. 2013 Mar 14. doi:pii: S1567-7249(13)00041-X. 10.1016/j.mito.2013.03.002. [Epub ahead of print] 2013
2MTFMT
Mutations in MTFMT underlie a human disorder of formylation causing impaired mitochondrial translation.
Tucker EJ, Hershman SG, Köhrer C, Belcher-Timme CA, Patel J, Goldberger OA, Christodoulou J, Silberstein JM, McKenzie M, Ryan MT, Compton AG, Jaffe JD, Carr SA, Calvo SE, RajBhandary UL, Thorburn DR, Mootha VK.
Cell Metab 14(3):428-34. doi: 10.1016/j.cmet.2011.07.010. 2011
3MTFMT
Mammalian mitochondrial methionyl-tRNA transformylase from bovine liver. Purification, characterization, and gene structure.
Takeuchi N, Kawakami M, Omori A, Ueda T, Spremulli LL, Watanabe K.
J Biol Chem 273(24):15085-90. 1998