Intra-mitochondrial Methylation Deficiency Due to Mutations in

We report a syndrome in three families affected by reduced intra-mitochondrial methylation caused by recessive mutations in the gene encoding the only known mitochondrial SAM transporter, SLC25A26.

Source: The American Journal of Human Genetics - October 29, 2015 Category: Genetics & Stem Cells Authors: Yoshihito Kishita, Aleksandra Pajak, Nikhita Ajit Bolar, Carlo M.T. Marobbio, Camilla Maffezzini, Daniela V. Miniero, Magnus Monné, Masakazu Kohda, Henrik Stranneheim, Kei Murayama, Karin Naess, Nicole Lesko, Helene Bruhn, Arnaud Mourier, Rolf Wibom, Tags: Report Source Type: research