| 1 | SAMD, SLC25A26 |
| Intra-mitochondrial Methylation Deficiency Due to Mutations in SLC25A26. | |
| Kishita Y, Pajak A, Bolar NA, Marobbio CM, Maffezzini C, Miniero DV, Monné M, Kohda M, Stranneheim H, Murayama K, Naess K, Lesko N, Bruhn H, Mourier A, Wibom R, Nennesmo I, Jespers A, Govaert P, Ohtake A, Van Laer L, Loeys BL, Freyer C, Palmieri F, Wredenberg A, Okazaki Y, Wedell A. | |
| Am J Hum Genet 97(5):761-8. doi: 10.1016/j.ajhg.2015.09.013. Epub 2015 Oct 29. 2015 | |
| 2 | SLC25A26 |
| The mitochondrial transporter family SLC25: identification, properties and physiopathology. | |
| Palmieri F. | |
| Mol Aspects Med 34(2-3):465-84. doi: 10.1016/j.mam.2012.05.005. Epub 2012 Dec 23. Review. 2013 | |
| 3 | SLC25A26 |
| Identification of the human mitochondrial S-adenosylmethionine transporter: bacterial expression, reconstitution, functional characterization and tissue distribution. | |
| Agrimi G, Di Noia MA, Marobbio CM, Fiermonte G, Lasorsa FM, Palmieri F. | |
| Biochem J 379(Pt 1):183-90. 2004 | |