| pubmed-article:18571778 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:18571778 | lifeskim:mentions | umls-concept:C0242422 | lld:lifeskim |
| pubmed-article:18571778 | lifeskim:mentions | umls-concept:C0017428 | lld:lifeskim |
| pubmed-article:18571778 | lifeskim:mentions | umls-concept:C0285890 | lld:lifeskim |
| pubmed-article:18571778 | lifeskim:mentions | umls-concept:C1261322 | lld:lifeskim |
| pubmed-article:18571778 | lifeskim:mentions | umls-concept:C2911648 | lld:lifeskim |
| pubmed-article:18571778 | pubmed:issue | 6 | lld:pubmed |
| pubmed-article:18571778 | pubmed:dateCreated | 2008-6-26 | lld:pubmed |
| pubmed-article:18571778 | pubmed:abstractText | Copy number variation is a common polymorphic phenomenon within the human genome. Although the majority of these events are non-deleterious they can also be highly pathogenic. Herein we characterize five families with parkinsonism that have been identified to harbor multiplication of the chromosomal 4q21 locus containing the alpha-synuclein gene (SNCA). | lld:pubmed |
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| pubmed-article:18571778 | pubmed:grant | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:18571778 | pubmed:language | eng | lld:pubmed |
| pubmed-article:18571778 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:18571778 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:18571778 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:18571778 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:18571778 | pubmed:month | Jun | lld:pubmed |
| pubmed-article:18571778 | pubmed:issn | 1531-8249 | lld:pubmed |
| pubmed-article:18571778 | pubmed:author | pubmed-author:RossOwen AOA | lld:pubmed |
| pubmed-article:18571778 | pubmed:author | pubmed-author:MaraganoreDem... | lld:pubmed |
| pubmed-article:18571778 | pubmed:author | pubmed-author:GasserThomasT | lld:pubmed |
| pubmed-article:18571778 | pubmed:author | pubmed-author:AdlerCharles... | lld:pubmed |
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| pubmed-article:18571778 | pubmed:author | pubmed-author:HattoriNobuta... | lld:pubmed |
| pubmed-article:18571778 | pubmed:author | pubmed-author:LangstonJ... | lld:pubmed |
| pubmed-article:18571778 | pubmed:author | pubmed-author:FarrerMatthew... | lld:pubmed |
| pubmed-article:18571778 | pubmed:author | pubmed-author:NilssonChrist... | lld:pubmed |
| pubmed-article:18571778 | pubmed:author | pubmed-author:Chartier-Harl... | lld:pubmed |
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| pubmed-article:18571778 | pubmed:author | pubmed-author:LarvorLydieL | lld:pubmed |
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| pubmed-article:18571778 | pubmed:author | pubmed-author:BraithwaiteAd... | lld:pubmed |
| pubmed-article:18571778 | pubmed:issnType | Electronic | lld:pubmed |
| pubmed-article:18571778 | pubmed:volume | 63 | lld:pubmed |
| pubmed-article:18571778 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:18571778 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:18571778 | pubmed:pagination | 743-50 | lld:pubmed |
| pubmed-article:18571778 | pubmed:dateRevised | 2011-9-22 | lld:pubmed |
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| pubmed-article:18571778 | pubmed:year | 2008 | lld:pubmed |
| pubmed-article:18571778 | pubmed:articleTitle | Genomic investigation of alpha-synuclein multiplication and parkinsonism. | lld:pubmed |
| pubmed-article:18571778 | pubmed:affiliation | Division of Neurogenetics, Department of Neuroscience, College of Medicine, Mayo Clinic, Jacksonville, FL 32224, USA. | lld:pubmed |
| pubmed-article:18571778 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:18571778 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
| pubmed-article:18571778 | pubmed:publicationType | Research Support, N.I.H., Extramural | lld:pubmed |
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