| pubmed-article:18638528 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:18638528 | lifeskim:mentions | umls-concept:C0032659 | lld:lifeskim |
| pubmed-article:18638528 | lifeskim:mentions | umls-concept:C0030567 | lld:lifeskim |
| pubmed-article:18638528 | lifeskim:mentions | umls-concept:C1421309 | lld:lifeskim |
| pubmed-article:18638528 | lifeskim:mentions | umls-concept:C0004083 | lld:lifeskim |
| pubmed-article:18638528 | lifeskim:mentions | umls-concept:C1882417 | lld:lifeskim |
| pubmed-article:18638528 | lifeskim:mentions | umls-concept:C0332120 | lld:lifeskim |
| pubmed-article:18638528 | pubmed:issue | 3 | lld:pubmed |
| pubmed-article:18638528 | pubmed:dateCreated | 2008-8-12 | lld:pubmed |
| pubmed-article:18638528 | pubmed:abstractText | Mutation in UCH-L1 has been reported as a rare cause of autosomal dominant Parkinson's disease (PD). A S18Y polymorphism in the same gene has been associated with sporadic PD. We investigated the frequency of this polymorphism among the Han-Chinese ethnic population in a case-control study. A total of 600 patients with PD and 334 unrelated healthy controls were genotyped using PCR-restriction fragment length polymorphism analysis. We did not observe any difference in allele or genotype frequencies between the cases and the controls (P>0.05). Our results do not support a role for this variant in sporadic PD. | lld:pubmed |
| pubmed-article:18638528 | pubmed:language | eng | lld:pubmed |
| pubmed-article:18638528 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:18638528 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:18638528 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:18638528 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:18638528 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:18638528 | pubmed:month | Sep | lld:pubmed |
| pubmed-article:18638528 | pubmed:issn | 0304-3940 | lld:pubmed |
| pubmed-article:18638528 | pubmed:author | pubmed-author:PennII | lld:pubmed |
| pubmed-article:18638528 | pubmed:author | pubmed-author:WuYY | lld:pubmed |
| pubmed-article:18638528 | pubmed:author | pubmed-author:SuY MYM | lld:pubmed |
| pubmed-article:18638528 | pubmed:author | pubmed-author:BurgunderJ-MJ... | lld:pubmed |
| pubmed-article:18638528 | pubmed:author | pubmed-author:ChenW-JWJ | lld:pubmed |
| pubmed-article:18638528 | pubmed:author | pubmed-author:ZhangZ-JZJ | lld:pubmed |
| pubmed-article:18638528 | pubmed:author | pubmed-author:WangY-CYC | lld:pubmed |
| pubmed-article:18638528 | pubmed:author | pubmed-author:ZhangJ-HJH | lld:pubmed |
| pubmed-article:18638528 | pubmed:author | pubmed-author:AnX-KXK | lld:pubmed |
| pubmed-article:18638528 | pubmed:author | pubmed-author:GouY-RYR | lld:pubmed |
| pubmed-article:18638528 | pubmed:author | pubmed-author:YuanG-GGG | lld:pubmed |
| pubmed-article:18638528 | pubmed:author | pubmed-author:MaoX-YXY | lld:pubmed |
| pubmed-article:18638528 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:18638528 | pubmed:day | 19 | lld:pubmed |
| pubmed-article:18638528 | pubmed:volume | 442 | lld:pubmed |
| pubmed-article:18638528 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:18638528 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:18638528 | pubmed:pagination | 200-2 | lld:pubmed |
| pubmed-article:18638528 | pubmed:meshHeading | pubmed-meshheading:18638528... | lld:pubmed |
| pubmed-article:18638528 | pubmed:meshHeading | pubmed-meshheading:18638528... | lld:pubmed |
| pubmed-article:18638528 | pubmed:meshHeading | pubmed-meshheading:18638528... | lld:pubmed |
| pubmed-article:18638528 | pubmed:meshHeading | pubmed-meshheading:18638528... | lld:pubmed |
| pubmed-article:18638528 | pubmed:meshHeading | pubmed-meshheading:18638528... | lld:pubmed |
| pubmed-article:18638528 | pubmed:meshHeading | pubmed-meshheading:18638528... | lld:pubmed |
| pubmed-article:18638528 | pubmed:meshHeading | pubmed-meshheading:18638528... | lld:pubmed |
| pubmed-article:18638528 | pubmed:meshHeading | pubmed-meshheading:18638528... | lld:pubmed |
| pubmed-article:18638528 | pubmed:meshHeading | pubmed-meshheading:18638528... | lld:pubmed |
| pubmed-article:18638528 | pubmed:meshHeading | pubmed-meshheading:18638528... | lld:pubmed |
| pubmed-article:18638528 | pubmed:meshHeading | pubmed-meshheading:18638528... | lld:pubmed |
| pubmed-article:18638528 | pubmed:meshHeading | pubmed-meshheading:18638528... | lld:pubmed |
| pubmed-article:18638528 | pubmed:meshHeading | pubmed-meshheading:18638528... | lld:pubmed |
| pubmed-article:18638528 | pubmed:meshHeading | pubmed-meshheading:18638528... | lld:pubmed |
| pubmed-article:18638528 | pubmed:year | 2008 | lld:pubmed |
| pubmed-article:18638528 | pubmed:articleTitle | Lack of evidence for association of a UCH-L1 S18Y polymorphism with Parkinson's disease in a Han-Chinese population. | lld:pubmed |
| pubmed-article:18638528 | pubmed:affiliation | Department of Neurology, West China Hospital, Sichuan University, Chengdu 610041, Chengdu, China. | lld:pubmed |
| pubmed-article:18638528 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:18638528 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
| entrez-gene:7345 | entrezgene:pubmed | pubmed-article:18638528 | lld:entrezgene |
| http://linkedlifedata.com/r... | entrezgene:pubmed | pubmed-article:18638528 | lld:entrezgene |
| http://linkedlifedata.com/r... | entrezgene:pubmed | pubmed-article:18638528 | lld:entrezgene |
| lhgdn:association:31837 | lhgdn:found_in | pubmed-article:18638528 | lld:lhgdn |
