Fatal infantile cardioencephalomyopathy with COX deficiency and mutations in SCO2, a COX assembly gene.Published in:Nature Genetics, 1999, v. 23, n. 3, p. 333, doi. 10.1038/15513By:Papadopoulou, Lefkothea C.;Sue, Carolyn M.;Davidson, Mercy M.;Tanji, Kurenai;Nishino, Ichizo;Sadlock, James E.;Krishna, Sindu;Walker, Winsome;Selby, Jeanette;Glerum, D. Moira;Coster, Rudy Van;Lyon, Gilles;Scalais, Emmanuel;Lebel, Roger;Kaplan, Paige;Shanske, Sara;De Vivo, Darryl C.;Bonilla, Eduardo;Hirano, MichioPublication type:Article