| pubmed-article:19038850 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:19038850 | lifeskim:mentions | umls-concept:C0019425 | lld:lifeskim |
| pubmed-article:19038850 | lifeskim:mentions | umls-concept:C0026882 | lld:lifeskim |
| pubmed-article:19038850 | lifeskim:mentions | umls-concept:C2936327 | lld:lifeskim |
| pubmed-article:19038850 | lifeskim:mentions | umls-concept:C0205245 | lld:lifeskim |
| pubmed-article:19038850 | lifeskim:mentions | umls-concept:C1422771 | lld:lifeskim |
| pubmed-article:19038850 | lifeskim:mentions | umls-concept:C0237876 | lld:lifeskim |
| pubmed-article:19038850 | lifeskim:mentions | umls-concept:C1742737 | lld:lifeskim |
| pubmed-article:19038850 | lifeskim:mentions | umls-concept:C0205214 | lld:lifeskim |
| pubmed-article:19038850 | pubmed:issue | 12 | lld:pubmed |
| pubmed-article:19038850 | pubmed:dateCreated | 2009-3-24 | lld:pubmed |
| pubmed-article:19038850 | pubmed:abstractText | To use a combined neurogenetic-neuroimaging approach to examine the functional consequences of preclinical dopaminergic nigrostriatal dysfunction in the human motor system. Specifically, we examined how a single heterozygous mutation in different genes associated with recessively inherited Parkinson disease alters the cortical control of sequential finger movements. | lld:pubmed |
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| pubmed-article:19038850 | pubmed:language | eng | lld:pubmed |
| pubmed-article:19038850 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:19038850 | pubmed:citationSubset | AIM | lld:pubmed |
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| pubmed-article:19038850 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:19038850 | pubmed:month | Mar | lld:pubmed |
| pubmed-article:19038850 | pubmed:issn | 1526-632X | lld:pubmed |
| pubmed-article:19038850 | pubmed:author | pubmed-author:WeissM MMM | lld:pubmed |
| pubmed-article:19038850 | pubmed:author | pubmed-author:KleinCC | lld:pubmed |
| pubmed-article:19038850 | pubmed:author | pubmed-author:LohmannKK | lld:pubmed |
| pubmed-article:19038850 | pubmed:author | pubmed-author:BloemB RBR | lld:pubmed |
| pubmed-article:19038850 | pubmed:author | pubmed-author:BinkofskiFF | lld:pubmed |
| pubmed-article:19038850 | pubmed:author | pubmed-author:SiebnerH RHR | lld:pubmed |
| pubmed-article:19038850 | pubmed:author | pubmed-author:HagenahJJ | lld:pubmed |
| pubmed-article:19038850 | pubmed:author | pubmed-author:PramstallerP... | lld:pubmed |
| pubmed-article:19038850 | pubmed:author | pubmed-author:ReetzKK | lld:pubmed |
| pubmed-article:19038850 | pubmed:author | pubmed-author:van EimerenTT | lld:pubmed |
| pubmed-article:19038850 | pubmed:author | pubmed-author:van NuenenB... | lld:pubmed |
| pubmed-article:19038850 | pubmed:issnType | Electronic | lld:pubmed |
| pubmed-article:19038850 | pubmed:day | 24 | lld:pubmed |
| pubmed-article:19038850 | pubmed:volume | 72 | lld:pubmed |
| pubmed-article:19038850 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:19038850 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:19038850 | pubmed:pagination | 1041-7 | lld:pubmed |
| pubmed-article:19038850 | pubmed:dateRevised | 2010-9-22 | lld:pubmed |
| pubmed-article:19038850 | pubmed:meshHeading | pubmed-meshheading:19038850... | lld:pubmed |
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| pubmed-article:19038850 | pubmed:meshHeading | pubmed-meshheading:19038850... | lld:pubmed |
| pubmed-article:19038850 | pubmed:meshHeading | pubmed-meshheading:19038850... | lld:pubmed |
| pubmed-article:19038850 | pubmed:meshHeading | pubmed-meshheading:19038850... | lld:pubmed |
| pubmed-article:19038850 | pubmed:meshHeading | pubmed-meshheading:19038850... | lld:pubmed |
| pubmed-article:19038850 | pubmed:meshHeading | pubmed-meshheading:19038850... | lld:pubmed |
| pubmed-article:19038850 | pubmed:meshHeading | pubmed-meshheading:19038850... | lld:pubmed |
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| pubmed-article:19038850 | pubmed:meshHeading | pubmed-meshheading:19038850... | lld:pubmed |
| pubmed-article:19038850 | pubmed:year | 2009 | lld:pubmed |
| pubmed-article:19038850 | pubmed:articleTitle | Heterozygous carriers of a Parkin or PINK1 mutation share a common functional endophenotype. | lld:pubmed |
| pubmed-article:19038850 | pubmed:affiliation | Department of Neurology, Christian-Albrechts University, Kiel, Germany. | lld:pubmed |
| pubmed-article:19038850 | pubmed:publicationType | Journal Article | lld:pubmed |
