Fatal infantile cardioencephalomyopathy with COX deficiency and mutations in SCO2, a COX assembly gene-Reference-Cited by-同舟云学术

Fatal infantile cardioencephalomyopathy with COX deficiency and mutations in SCO2, a COX assembly gene

Published:1999-11 Issue:3 Volume:23 Page:333-337
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

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 Michio,DiMauro Salvatore,Schon Eric A.

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng1199_333.pdf

Reference29 articles.

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3. Glerum, D.M. & Tzagoloff, A. Isolation of a human cDNA for heme A:farnesyltransferase by functional complementation of a yeast cox10 mutant. Proc. Natl Acad. Sci. USA 91, 8452–8456 (1994).

4. Petruzzella, V. et al. Identification and characterization of human cDNAs specific to BCS1, PET112, SCO1, COX15, and COX11, five genes involved in the formation and function of the mitochondrial respiratory chain. Genomics 15, 494– 504 (1998).

5. Amaravadi, R., Glerum, D.M. & Tzagoloff, A. Isolation of a cDNA encoding the human homolog of COX17, a yeast gene essential for mitochondrial copper recruitment. Hum. Genet. 99, 329–333 (1997).

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