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Nicholls, Zsurka, Peeva, Schöler, Szczesny, Cysewski, Reyes, Kornblum, Sciacco, Moggio, Dziembowski, Kunz, Minczuk: "Linear mtDNA fragments and unusual mtDNA rearrangements associated with pathological deficiency of MGME1 exonuclease." in: Human molecular genetics, Vol. 23, Issue 23, pp. 6147-62, (2014) (PubMed).
Kornblum, Nicholls, Haack, Schöler, Peeva, Danhauser, Hallmann, Zsurka, Rorbach, Iuso, Wieland, Sciacco, Ronchi, Comi, Moggio, Quinzii, DiMauro, Calvo, Mootha, Klopstock, Strom, Meitinger, Minczuk et al.: "Loss-of-function mutations in MGME1 impair mtDNA replication and cause multisystemic mitochondrial disease. ..." in: Nature genetics, Vol. 45, Issue 2, pp. 214-9, (2013) (PubMed).
Szczesny, Hejnowicz, Steczkiewicz, Muszewska, Borowski, Ginalski, Dziembowski: "Identification of a novel human mitochondrial endo-/exonuclease Ddk1/c20orf72 necessary for maintenance of proper 7S DNA levels." in: Nucleic acids research, Vol. 41, Issue 5, pp. 3144-61, (2013) (PubMed).
Synonyms and alternative names related to C20orf72