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| pubmed-article:17620546 | lifeskim:mentions | umls-concept:C0205314 | lld:lifeskim |
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| pubmed-article:17620546 | pubmed:dateCreated | 2007-7-10 | lld:pubmed |
| pubmed-article:17620546 | pubmed:abstractText | Frontotemporal dementia (FTD) in several 17q21-linked families was recently explained by truncating mutations in the progranulin gene (GRN). | lld:pubmed |
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| pubmed-article:17620546 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:17620546 | pubmed:month | Jul | lld:pubmed |
| pubmed-article:17620546 | pubmed:issn | 1526-632X | lld:pubmed |
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| pubmed-article:17620546 | pubmed:volume | 69 | lld:pubmed |
| pubmed-article:17620546 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:17620546 | pubmed:authorsComplete | Y | lld:pubmed |
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| pubmed-article:17620546 | pubmed:dateRevised | 2009-11-19 | lld:pubmed |
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| pubmed-article:17620546 | pubmed:year | 2007 | lld:pubmed |
| pubmed-article:17620546 | pubmed:articleTitle | Heterogeneity within a large kindred with frontotemporal dementia: a novel progranulin mutation. | lld:pubmed |
| pubmed-article:17620546 | pubmed:affiliation | Regional Neurogenetic Centre, Lamezia Terme, CZ, Italy. bruni@arn.it | lld:pubmed |
| pubmed-article:17620546 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:17620546 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
| pubmed-article:17620546 | pubmed:publicationType | Research Support, N.I.H., Intramural | lld:pubmed |
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