| pubmed-article:21270637 | rdf:type | pubmed:Citation | lld:pubmed |
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| pubmed-article:21270637 | lifeskim:mentions | umls-concept:C0005768 | lld:lifeskim |
| pubmed-article:21270637 | lifeskim:mentions | umls-concept:C0242422 | lld:lifeskim |
| pubmed-article:21270637 | lifeskim:mentions | umls-concept:C0521451 | lld:lifeskim |
| pubmed-article:21270637 | lifeskim:mentions | umls-concept:C0277785 | lld:lifeskim |
| pubmed-article:21270637 | lifeskim:mentions | umls-concept:C0600688 | lld:lifeskim |
| pubmed-article:21270637 | lifeskim:mentions | umls-concept:C0332281 | lld:lifeskim |
| pubmed-article:21270637 | lifeskim:mentions | umls-concept:C1414649 | lld:lifeskim |
| pubmed-article:21270637 | lifeskim:mentions | umls-concept:C1706937 | lld:lifeskim |
| pubmed-article:21270637 | lifeskim:mentions | umls-concept:C1519595 | lld:lifeskim |
| pubmed-article:21270637 | lifeskim:mentions | umls-concept:C0332120 | lld:lifeskim |
| pubmed-article:21270637 | pubmed:issue | 5 | lld:pubmed |
| pubmed-article:21270637 | pubmed:dateCreated | 2011-5-10 | lld:pubmed |
| pubmed-article:21270637 | pubmed:abstractText | Our previous results showed that both gray zone and lower end premutation range (40-85 repeats) fragile X mental retardation 1 (FMR1) alleles were more common among males with parkinsonism than in the general population. This study aimed to determine whether these alleles have a significant role in the manifestations and pathogenesis of parkinsonian disorders. | lld:pubmed |
| pubmed-article:21270637 | pubmed:grant | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21270637 | pubmed:grant | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21270637 | pubmed:language | eng | lld:pubmed |
| pubmed-article:21270637 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21270637 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:21270637 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21270637 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:21270637 | pubmed:month | May | lld:pubmed |
| pubmed-article:21270637 | pubmed:issn | 1530-0366 | lld:pubmed |
| pubmed-article:21270637 | pubmed:author | pubmed-author:EvansAndrewA | lld:pubmed |
| pubmed-article:21270637 | pubmed:author | pubmed-author:TrostNicholas... | lld:pubmed |
| pubmed-article:21270637 | pubmed:author | pubmed-author:StoreyElsdonE | lld:pubmed |
| pubmed-article:21270637 | pubmed:author | pubmed-author:FrancisDavidD | lld:pubmed |
| pubmed-article:21270637 | pubmed:author | pubmed-author:KinsellaGlynd... | lld:pubmed |
| pubmed-article:21270637 | pubmed:author | pubmed-author:LoeschDanuta... | lld:pubmed |
| pubmed-article:21270637 | pubmed:author | pubmed-author:BuiQuang MQM | lld:pubmed |
| pubmed-article:21270637 | pubmed:author | pubmed-author:VennAlisonA | lld:pubmed |
| pubmed-article:21270637 | pubmed:author | pubmed-author:ThorburnDavid... | lld:pubmed |
| pubmed-article:21270637 | pubmed:author | pubmed-author:SlaterHoward... | lld:pubmed |
| pubmed-article:21270637 | pubmed:author | pubmed-author:HorneMalcolmM | lld:pubmed |
| pubmed-article:21270637 | pubmed:author | pubmed-author:KotschetKatya... | lld:pubmed |
| pubmed-article:21270637 | pubmed:author | pubmed-author:GodlerDavid... | lld:pubmed |
| pubmed-article:21270637 | pubmed:author | pubmed-author:GehlingFreyaF | lld:pubmed |
| pubmed-article:21270637 | pubmed:author | pubmed-author:StimpsonPaige... | lld:pubmed |
| pubmed-article:21270637 | pubmed:issnType | Electronic | lld:pubmed |
| pubmed-article:21270637 | pubmed:volume | 13 | lld:pubmed |
| pubmed-article:21270637 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:21270637 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:21270637 | pubmed:pagination | 392-9 | lld:pubmed |
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| pubmed-article:21270637 | pubmed:meshHeading | pubmed-meshheading:21270637... | lld:pubmed |
| pubmed-article:21270637 | pubmed:meshHeading | pubmed-meshheading:21270637... | lld:pubmed |
| pubmed-article:21270637 | pubmed:meshHeading | pubmed-meshheading:21270637... | lld:pubmed |
| pubmed-article:21270637 | pubmed:meshHeading | pubmed-meshheading:21270637... | lld:pubmed |
| pubmed-article:21270637 | pubmed:meshHeading | pubmed-meshheading:21270637... | lld:pubmed |
| pubmed-article:21270637 | pubmed:meshHeading | pubmed-meshheading:21270637... | lld:pubmed |
| pubmed-article:21270637 | pubmed:year | 2011 | lld:pubmed |
| pubmed-article:21270637 | pubmed:articleTitle | Evidence for the toxicity of bidirectional transcripts and mitochondrial dysfunction in blood associated with small CGG expansions in the FMR1 gene in patients with parkinsonism. | lld:pubmed |
| pubmed-article:21270637 | pubmed:affiliation | School of Psychological Science, La Trobe University, Melbourne, Victoria, Australia. d.loesch@latrobe.edu.au | lld:pubmed |
| pubmed-article:21270637 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:21270637 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
| pubmed-article:21270637 | pubmed:publicationType | Research Support, N.I.H., Extramural | lld:pubmed |
| entrez-gene:2332 | entrezgene:pubmed | pubmed-article:21270637 | lld:entrezgene |
| http://linkedlifedata.com/r... | entrezgene:pubmed | pubmed-article:21270637 | lld:entrezgene |
