| pubmed-article:21060018 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:21060018 | lifeskim:mentions | umls-concept:C0497327 | lld:lifeskim |
| pubmed-article:21060018 | lifeskim:mentions | umls-concept:C0524851 | lld:lifeskim |
| pubmed-article:21060018 | lifeskim:mentions | umls-concept:C1856060 | lld:lifeskim |
| pubmed-article:21060018 | lifeskim:mentions | umls-concept:C0026882 | lld:lifeskim |
| pubmed-article:21060018 | lifeskim:mentions | umls-concept:C0521451 | lld:lifeskim |
| pubmed-article:21060018 | lifeskim:mentions | umls-concept:C0031453 | lld:lifeskim |
| pubmed-article:21060018 | lifeskim:mentions | umls-concept:C0035711 | lld:lifeskim |
| pubmed-article:21060018 | lifeskim:mentions | umls-concept:C0332281 | lld:lifeskim |
| pubmed-article:21060018 | lifeskim:mentions | umls-concept:C0205329 | lld:lifeskim |
| pubmed-article:21060018 | lifeskim:mentions | umls-concept:C1880022 | lld:lifeskim |
| pubmed-article:21060018 | pubmed:issue | 11 | lld:pubmed |
| pubmed-article:21060018 | pubmed:dateCreated | 2010-11-9 | lld:pubmed |
| pubmed-article:21060018 | pubmed:abstractText | Mitochondrial diseases are characterized by wide phenotypic and genetic variability, but presentations in adults with akinetic rigidity and hyperkinetic movement disorders are rare. | lld:pubmed |
| pubmed-article:21060018 | pubmed:grant | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21060018 | pubmed:grant | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21060018 | pubmed:language | eng | lld:pubmed |
| pubmed-article:21060018 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21060018 | pubmed:citationSubset | AIM | lld:pubmed |
| pubmed-article:21060018 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21060018 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21060018 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:21060018 | pubmed:month | Nov | lld:pubmed |
| pubmed-article:21060018 | pubmed:issn | 1538-3687 | lld:pubmed |
| pubmed-article:21060018 | pubmed:author | pubmed-author:TaylorRobert... | lld:pubmed |
| pubmed-article:21060018 | pubmed:author | pubmed-author:TurnbullDougl... | lld:pubmed |
| pubmed-article:21060018 | pubmed:author | pubmed-author:CarterJanet... | lld:pubmed |
| pubmed-article:21060018 | pubmed:author | pubmed-author:BlakelyEmma... | lld:pubmed |
| pubmed-article:21060018 | pubmed:author | pubmed-author:de... | lld:pubmed |
| pubmed-article:21060018 | pubmed:author | pubmed-author:KartsounisLuk... | lld:pubmed |
| pubmed-article:21060018 | pubmed:author | pubmed-author:YoungTim MTM | lld:pubmed |
| pubmed-article:21060018 | pubmed:author | pubmed-author:O'DonovanDomi... | lld:pubmed |
| pubmed-article:21060018 | pubmed:author | pubmed-author:SwalwellHelen... | lld:pubmed |
| pubmed-article:21060018 | pubmed:issnType | Electronic | lld:pubmed |
| pubmed-article:21060018 | pubmed:volume | 67 | lld:pubmed |
| pubmed-article:21060018 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:21060018 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:21060018 | pubmed:pagination | 1399-402 | lld:pubmed |
| pubmed-article:21060018 | pubmed:dateRevised | 2011-1-5 | lld:pubmed |
| pubmed-article:21060018 | pubmed:meshHeading | pubmed-meshheading:21060018... | lld:pubmed |
| pubmed-article:21060018 | pubmed:meshHeading | pubmed-meshheading:21060018... | lld:pubmed |
| pubmed-article:21060018 | pubmed:meshHeading | pubmed-meshheading:21060018... | lld:pubmed |
| pubmed-article:21060018 | pubmed:meshHeading | pubmed-meshheading:21060018... | lld:pubmed |
| pubmed-article:21060018 | pubmed:meshHeading | pubmed-meshheading:21060018... | lld:pubmed |
| pubmed-article:21060018 | pubmed:meshHeading | pubmed-meshheading:21060018... | lld:pubmed |
| pubmed-article:21060018 | pubmed:meshHeading | pubmed-meshheading:21060018... | lld:pubmed |
| pubmed-article:21060018 | pubmed:meshHeading | pubmed-meshheading:21060018... | lld:pubmed |
| pubmed-article:21060018 | pubmed:meshHeading | pubmed-meshheading:21060018... | lld:pubmed |
| pubmed-article:21060018 | pubmed:meshHeading | pubmed-meshheading:21060018... | lld:pubmed |
| pubmed-article:21060018 | pubmed:meshHeading | pubmed-meshheading:21060018... | lld:pubmed |
| pubmed-article:21060018 | pubmed:meshHeading | pubmed-meshheading:21060018... | lld:pubmed |
| pubmed-article:21060018 | pubmed:meshHeading | pubmed-meshheading:21060018... | lld:pubmed |
| pubmed-article:21060018 | pubmed:meshHeading | pubmed-meshheading:21060018... | lld:pubmed |
| pubmed-article:21060018 | pubmed:meshHeading | pubmed-meshheading:21060018... | lld:pubmed |
| pubmed-article:21060018 | pubmed:year | 2010 | lld:pubmed |
| pubmed-article:21060018 | pubmed:articleTitle | Mitochondrial transfer RNA(Phe) mutation associated with a progressive neurodegenerative disorder characterized by psychiatric disturbance, dementia, and akinesia-rigidity. | lld:pubmed |
| pubmed-article:21060018 | pubmed:affiliation | Essex Centre for Neurological Sciences, Queen's Hospital, Romford RM7 0AG, United Kingdom. | lld:pubmed |
| pubmed-article:21060018 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:21060018 | pubmed:publicationType | Case Reports | lld:pubmed |
| pubmed-article:21060018 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
