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| pubmed-article:14985393 | pubmed:issue | 3 | lld:pubmed |
| pubmed-article:14985393 | pubmed:dateCreated | 2004-2-26 | lld:pubmed |
| pubmed-article:14985393 | pubmed:language | eng | lld:pubmed |
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| pubmed-article:14985393 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:14985393 | pubmed:month | Mar | lld:pubmed |
| pubmed-article:14985393 | pubmed:issn | 1468-6244 | lld:pubmed |
| pubmed-article:14985393 | pubmed:author | pubmed-author:MashD CDC | lld:pubmed |
| pubmed-article:14985393 | pubmed:author | pubmed-author:WilkerJJ | lld:pubmed |
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| pubmed-article:14985393 | pubmed:author | pubmed-author:LincolnSS | lld:pubmed |
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| pubmed-article:14985393 | pubmed:author | pubmed-author:BisceglioGG | lld:pubmed |
| pubmed-article:14985393 | pubmed:author | pubmed-author:HulihanMM | lld:pubmed |
| pubmed-article:14985393 | pubmed:author | pubmed-author:KachergusJJ | lld:pubmed |
| pubmed-article:14985393 | pubmed:issnType | Electronic | lld:pubmed |
| pubmed-article:14985393 | pubmed:volume | 41 | lld:pubmed |
| pubmed-article:14985393 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:14985393 | pubmed:authorsComplete | Y | lld:pubmed |
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| pubmed-article:14985393 | pubmed:dateRevised | 2008-11-20 | lld:pubmed |
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| pubmed-article:14985393 | pubmed:year | 2004 | lld:pubmed |
| pubmed-article:14985393 | pubmed:articleTitle | DJ-1 mutations are a rare cause of recessively inherited early onset parkinsonism mediated by loss of protein function. | lld:pubmed |
| pubmed-article:14985393 | pubmed:publicationType | Letter | lld:pubmed |
| pubmed-article:14985393 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
| pubmed-article:14985393 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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