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pubmed-article:17400793 | lifeskim:mentions | umls-concept:C0012929 | lld:lifeskim |
pubmed-article:17400793 | lifeskim:mentions | umls-concept:C1537994 | lld:lifeskim |
pubmed-article:17400793 | lifeskim:mentions | umls-concept:C0030013 | lld:lifeskim |
pubmed-article:17400793 | lifeskim:mentions | umls-concept:C1524003 | lld:lifeskim |
pubmed-article:17400793 | lifeskim:mentions | umls-concept:C0332183 | lld:lifeskim |
pubmed-article:17400793 | lifeskim:mentions | umls-concept:C1711351 | lld:lifeskim |
pubmed-article:17400793 | pubmed:issue | 4 | lld:pubmed |
pubmed-article:17400793 | pubmed:dateCreated | 2007-4-2 | lld:pubmed |
pubmed-article:17400793 | pubmed:abstractText | Detection of mutations in the mitochondrial DNA (mtDNA) is usually limited to common mutations and the transfer RNA genes. However, mutations in other mtDNA regions can be an important cause of oxidative phosphorylation (OXPHOS) disease as well. | lld:pubmed |
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pubmed-article:17400793 | pubmed:language | eng | lld:pubmed |
pubmed-article:17400793 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:17400793 | pubmed:citationSubset | IM | lld:pubmed |
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pubmed-article:17400793 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:17400793 | pubmed:month | Apr | lld:pubmed |
pubmed-article:17400793 | pubmed:issn | 1468-6244 | lld:pubmed |
pubmed-article:17400793 | pubmed:author | pubmed-author:HendrickxAA | lld:pubmed |
pubmed-article:17400793 | pubmed:author | pubmed-author:SmeetsH JHJ | lld:pubmed |
pubmed-article:17400793 | pubmed:author | pubmed-author:Schoonderwoer... | lld:pubmed |
pubmed-article:17400793 | pubmed:author | pubmed-author:BlomM LML | lld:pubmed |
pubmed-article:17400793 | pubmed:author | pubmed-author:SpruijtLL | lld:pubmed |
pubmed-article:17400793 | pubmed:author | pubmed-author:de CooI F MIF | lld:pubmed |
pubmed-article:17400793 | pubmed:issnType | Electronic | lld:pubmed |
pubmed-article:17400793 | pubmed:volume | 44 | lld:pubmed |
pubmed-article:17400793 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:17400793 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:17400793 | pubmed:pagination | e74 | lld:pubmed |
pubmed-article:17400793 | pubmed:dateRevised | 2010-11-18 | lld:pubmed |
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pubmed-article:17400793 | pubmed:year | 2007 | lld:pubmed |
pubmed-article:17400793 | pubmed:articleTitle | Mutations in the ND5 subunit of complex I of the mitochondrial DNA are a frequent cause of oxidative phosphorylation disease. | lld:pubmed |
pubmed-article:17400793 | pubmed:affiliation | Department of Clinical Genetics, University Hospital, Maastricht, The Netherlands. rien.blok@gen.unimaas.nl | lld:pubmed |
pubmed-article:17400793 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:17400793 | pubmed:publicationType | Case Reports | lld:pubmed |
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