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cite-note-1616. ↑ citerefknuffaberhuthfreisinger2007Knuf M, Faber J, Huth RG, Freisinger P, Zepp F, Kampmann C (January 2007). "Identification of a novel compound heterozygote SCO2 mutation in cytochrome c oxidase deficient fatal infantile cardioencephalomyopathy". Acta Paediatrica. 96 (1): 130–2. doi:10.1111/j.1651-2227.2007.00008.x. PMID 17187620. S2CID 20422657.

cite-note-1717. ↑ citerefsalviatisacconirasalankronn2002Salviati L, Sacconi S, Rasalan MM, Kronn DF, Braun A, Canoll P, Davidson M, Shanske S, Bonilla E, Hays AP, Schon EA, DiMauro S (May 2002). "Cytochrome c oxidase deficiency due to a novel SCO2 mutation mimics Werdnig-Hoffmann disease". Archives of Neurology. 59 (5): 862–5. doi:10.1001/archneur.59.5.862. PMID 12020273.

cite-note-1818. ↑ citereftayshanskekaplandimauro2004Tay SK, Shanske S, Kaplan P, DiMauro S (June 2004). "Association of mutations in SCO2, a cytochrome c oxidase assembly gene, with early fetal lethality". Archives of Neurology. 61 (6): 950–2. doi:10.1001/archneur.61.6.950. PMID 15210538.

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