pubmed-article:10993999 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:10993999 | lifeskim:mentions | umls-concept:C0152035 | lld:lifeskim |
pubmed-article:10993999 | lifeskim:mentions | umls-concept:C0242422 | lld:lifeskim |
pubmed-article:10993999 | lifeskim:mentions | umls-concept:C0752121 | lld:lifeskim |
pubmed-article:10993999 | lifeskim:mentions | umls-concept:C0680174 | lld:lifeskim |
pubmed-article:10993999 | pubmed:issue | 6 | lld:pubmed |
pubmed-article:10993999 | pubmed:dateCreated | 2000-10-4 | lld:pubmed |
pubmed-article:10993999 | pubmed:abstractText | To describe the clinical and molecular genetic analysis of a large family of northern Chinese descent with a mutation at the SCA2 locus causing carbidopa-levodopa-responsive parkinsonism. | lld:pubmed |
pubmed-article:10993999 | pubmed:language | eng | lld:pubmed |
pubmed-article:10993999 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:10993999 | pubmed:citationSubset | AIM | lld:pubmed |
pubmed-article:10993999 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:10993999 | pubmed:month | Sep | lld:pubmed |
pubmed-article:10993999 | pubmed:issn | 0028-3878 | lld:pubmed |
pubmed-article:10993999 | pubmed:author | pubmed-author:ChenJ YJY | lld:pubmed |
pubmed-article:10993999 | pubmed:author | pubmed-author:AdamAA | lld:pubmed |
pubmed-article:10993999 | pubmed:author | pubmed-author:KAUQ YQY | lld:pubmed |
pubmed-article:10993999 | pubmed:author | pubmed-author:HardyJJ | lld:pubmed |
pubmed-article:10993999 | pubmed:author | pubmed-author:LiuH CHC | lld:pubmed |
pubmed-article:10993999 | pubmed:author | pubmed-author:WatersCC | lld:pubmed |
pubmed-article:10993999 | pubmed:author | pubmed-author:BossMM | lld:pubmed |
pubmed-article:10993999 | pubmed:author | pubmed-author:SingletonAA | lld:pubmed |
pubmed-article:10993999 | pubmed:author | pubmed-author:FarrerMM | lld:pubmed |
pubmed-article:10993999 | pubmed:author | pubmed-author:SeltzerWW | lld:pubmed |
pubmed-article:10993999 | pubmed:author | pubmed-author:KoroshetzWW | lld:pubmed |
pubmed-article:10993999 | pubmed:author | pubmed-author:Gwinn-HardyKK | lld:pubmed |
pubmed-article:10993999 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:10993999 | pubmed:day | 26 | lld:pubmed |
pubmed-article:10993999 | pubmed:volume | 55 | lld:pubmed |
pubmed-article:10993999 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:10993999 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:10993999 | pubmed:pagination | 800-5 | lld:pubmed |
pubmed-article:10993999 | pubmed:dateRevised | 2006-11-15 | lld:pubmed |
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pubmed-article:10993999 | pubmed:meshHeading | pubmed-meshheading:10993999... | lld:pubmed |
pubmed-article:10993999 | pubmed:year | 2000 | lld:pubmed |
pubmed-article:10993999 | pubmed:articleTitle | Spinocerebellar ataxia type 2 with parkinsonism in ethnic Chinese. | lld:pubmed |
pubmed-article:10993999 | pubmed:affiliation | Departments of Neurology and Pharmacology, Mayo Clinic Jacksonville, FL 32224, USA. gwinn.katrina@mayo.edu | lld:pubmed |
pubmed-article:10993999 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:10993999 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
pubmed-article:10993999 | pubmed:publicationType | Case Reports | lld:pubmed |
pubmed-article:10993999 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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