pubmed-article:19139307 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:19139307 | lifeskim:mentions | umls-concept:C0439660 | lld:lifeskim |
pubmed-article:19139307 | lifeskim:mentions | umls-concept:C0242422 | lld:lifeskim |
pubmed-article:19139307 | lifeskim:mentions | umls-concept:C0285890 | lld:lifeskim |
pubmed-article:19139307 | lifeskim:mentions | umls-concept:C0031437 | lld:lifeskim |
pubmed-article:19139307 | lifeskim:mentions | umls-concept:C0017287 | lld:lifeskim |
pubmed-article:19139307 | lifeskim:mentions | umls-concept:C0376249 | lld:lifeskim |
pubmed-article:19139307 | lifeskim:mentions | umls-concept:C0441712 | lld:lifeskim |
pubmed-article:19139307 | pubmed:issue | 1 | lld:pubmed |
pubmed-article:19139307 | pubmed:dateCreated | 2009-1-13 | lld:pubmed |
pubmed-article:19139307 | pubmed:abstractText | Genomic multiplications of the alpha-synuclein gene (SNCA) cause autosomal dominant Parkinson disease (ADPD). The aim of this study was to assess the frequency and phenotype of SNCA rearrangements in a large series of families with typical or atypical AD parkinsonism. | lld:pubmed |
pubmed-article:19139307 | pubmed:language | eng | lld:pubmed |
pubmed-article:19139307 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:19139307 | pubmed:citationSubset | AIM | lld:pubmed |
pubmed-article:19139307 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:19139307 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:19139307 | pubmed:month | Jan | lld:pubmed |
pubmed-article:19139307 | pubmed:issn | 1538-3687 | lld:pubmed |
pubmed-article:19139307 | pubmed:author | pubmed-author:French... | lld:pubmed |
pubmed-article:19139307 | pubmed:author | pubmed-author:DürrAlexandra... | lld:pubmed |
pubmed-article:19139307 | pubmed:author | pubmed-author:BriceAlexisA | lld:pubmed |
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pubmed-article:19139307 | pubmed:author | pubmed-author:DestéeAlainA | lld:pubmed |
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pubmed-article:19139307 | pubmed:author | pubmed-author:DurifFrankF | lld:pubmed |
pubmed-article:19139307 | pubmed:issnType | Electronic | lld:pubmed |
pubmed-article:19139307 | pubmed:volume | 66 | lld:pubmed |
pubmed-article:19139307 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:19139307 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:19139307 | pubmed:pagination | 102-8 | lld:pubmed |
pubmed-article:19139307 | pubmed:dateRevised | 2009-11-19 | lld:pubmed |
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pubmed-article:19139307 | pubmed:year | 2009 | lld:pubmed |
pubmed-article:19139307 | pubmed:articleTitle | Alpha-synuclein gene rearrangements in dominantly inherited parkinsonism: frequency, phenotype, and mechanisms. | lld:pubmed |
pubmed-article:19139307 | pubmed:affiliation | Institut National de la Santé et de la Recherche Médicale (INSERM), Unité Mixte de Recherche en Santé (UMR)_S679 Neurologie & Thérapeutique Expérimentale, F-75013, Paris, France. | lld:pubmed |
pubmed-article:19139307 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:19139307 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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