reference/20798459

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endingPage	3439
issn	1460-2083 0964-6906
issueIdentifier	17
pageRange	3430-3439
publicationName	Human Molecular Genetics
startingPage	3430
bibliographicCitation	Mayr JA, Havlícková V, Zimmermann F, Magler I, Kaplanová V, Jesina P, Pecinová A, Nusková H, Koch J, Sperl W, Houstek J. Mitochondrial ATP synthase deficiency due to a mutation in the ATP5E gene for the F1 epsilon subunit. Hum Mol Genet. 2010 Sep 01;19(17):3430–9. doi: 10.1093/hmg/ddq254. PMID: 20566710.
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date	2010-06-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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title	Mitochondrial ATP synthase deficiency due to a mutation in the ATP5E gene for the F1 epsilon subunit
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