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pubmed-article:16145815 | pubmed:issue | 2 | lld:pubmed |
pubmed-article:16145815 | pubmed:dateCreated | 2005-9-7 | lld:pubmed |
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pubmed-article:16145815 | pubmed:language | eng | lld:pubmed |
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pubmed-article:16145815 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:16145815 | pubmed:month | Aug | lld:pubmed |
pubmed-article:16145815 | pubmed:issn | 0002-9297 | lld:pubmed |
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pubmed-article:16145815 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:16145815 | pubmed:volume | 77 | lld:pubmed |
pubmed-article:16145815 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:16145815 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:16145815 | pubmed:pagination | 330-2 | lld:pubmed |
pubmed-article:16145815 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
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pubmed-article:16145815 | pubmed:year | 2005 | lld:pubmed |
pubmed-article:16145815 | pubmed:articleTitle | LRRK2 haplotype analyses in European and North African families with Parkinson disease: a common founder for the G2019S mutation dating from the 13th century. | lld:pubmed |
pubmed-article:16145815 | pubmed:publicationType | Letter | lld:pubmed |
pubmed-article:16145815 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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