| pubmed-article:17923635 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:17923635 | lifeskim:mentions | umls-concept:C1705387 | lld:lifeskim |
| pubmed-article:17923635 | lifeskim:mentions | umls-concept:C1842937 | lld:lifeskim |
| pubmed-article:17923635 | lifeskim:mentions | umls-concept:C0242422 | lld:lifeskim |
| pubmed-article:17923635 | lifeskim:mentions | umls-concept:C0752121 | lld:lifeskim |
| pubmed-article:17923635 | lifeskim:mentions | umls-concept:C1512900 | lld:lifeskim |
| pubmed-article:17923635 | pubmed:issue | 10 | lld:pubmed |
| pubmed-article:17923635 | pubmed:dateCreated | 2007-10-9 | lld:pubmed |
| pubmed-article:17923635 | pubmed:abstractText | To examine the presence of an ATXN2 mutation in patients with parkinsonism in the Korean population and to find the difference in the ATXN2 mutation between ataxic and parkinsonian phenotypes. | lld:pubmed |
| pubmed-article:17923635 | pubmed:language | eng | lld:pubmed |
| pubmed-article:17923635 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:17923635 | pubmed:citationSubset | AIM | lld:pubmed |
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| pubmed-article:17923635 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:17923635 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:17923635 | pubmed:month | Oct | lld:pubmed |
| pubmed-article:17923635 | pubmed:issn | 0003-9942 | lld:pubmed |
| pubmed-article:17923635 | pubmed:author | pubmed-author:KimYu... | lld:pubmed |
| pubmed-article:17923635 | pubmed:author | pubmed-author:ParkSung... | lld:pubmed |
| pubmed-article:17923635 | pubmed:author | pubmed-author:KimJong-MinJM | lld:pubmed |
| pubmed-article:17923635 | pubmed:author | pubmed-author:JeonBeom SBS | lld:pubmed |
| pubmed-article:17923635 | pubmed:author | pubmed-author:KimSang EunSE | lld:pubmed |
| pubmed-article:17923635 | pubmed:author | pubmed-author:HongSusieS | lld:pubmed |
| pubmed-article:17923635 | pubmed:author | pubmed-author:KimGyoung... | lld:pubmed |
| pubmed-article:17923635 | pubmed:author | pubmed-author:ChoiYoon... | lld:pubmed |
| pubmed-article:17923635 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:17923635 | pubmed:volume | 64 | lld:pubmed |
| pubmed-article:17923635 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:17923635 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:17923635 | pubmed:pagination | 1510-8 | lld:pubmed |
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| pubmed-article:17923635 | pubmed:year | 2007 | lld:pubmed |
| pubmed-article:17923635 | pubmed:articleTitle | Importance of low-range CAG expansion and CAA interruption in SCA2 Parkinsonism. | lld:pubmed |
| pubmed-article:17923635 | pubmed:affiliation | Department of Neurology, Seoul National University Hospital, Seoul 110-744, South Korea. | lld:pubmed |
| pubmed-article:17923635 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:17923635 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
| entrez-gene:6311 | entrezgene:pubmed | pubmed-article:17923635 | lld:entrezgene |
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| http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:17923635 | lld:pubmed |
