O.24 Loss of function of MGME1, a novel player in mitochondrial DNA replication, causes a distinct autosomal recessive mitochondrial disorder

✍ Scribed by Kornblum, C.; Nicholls, T.; Haack, T.B.; Schoeler, S.; Peeva, V.; Danhauser, K.; Hallmann, K.; Zsurka, G.; Rorbach, J.; Iuso, A.; Wieland, T.; Sciacco, M.; Ronchi, D.; Comi, G.P.; Moggio, M.; Quinzii, C.M.; DiMauro, S.; Calvo, S.E.; Mootha, V.K.; Klopstock, T.; Strom, T.M.; Meitinger, T.; Minczuk, M.; Kunz, W.S.; Prokisch, H.

• Book ID: 122086902
• Publisher: Elsevier Science
• Year: 2013
• Tongue: English
• Weight: 42 KB
• Volume: 23
• Category: Article
• ISSN: 0960-8966
• DOI: 10.1016/j.nmd.2013.06.734