reference/22636904

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/22636904

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endingPage	2702
issn	1460-2083
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pageRange	2693-2702
publicationName	Human Molecular Genetics
startingPage	2693
bibliographicCitation	Antonicka H, Leary SC, Guercin GH, Agar JN, Horvath R, Kennaway NG, Harding CO, Jaksch M, Shoubridge EA. Mutations in COX10 result in a defect in mitochondrial heme A biosynthesis and account for multiple, early-onset clinical phenotypes associated with isolated COX deficiency. Hum Mol Genet. 2003 Oct 15;12(20):2693–702. doi: 10.1093/hmg/ddg284. PMID: 12928484.
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date	2003-08-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://pubmed.ncbi.nlm.nih.gov/12928484 https://doi.org/10.1093/hmg/ddg284
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language	English
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title	Mutations in COX10 result in a defect in mitochondrial heme A biosynthesis and account for multiple, early-onset clinical phenotypes associated with isolated COX deficiency
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