|
rdf:type |
|
|
lifeskim:mentions |
|
|
pubmed:issue |
9
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|
pubmed:dateCreated |
2005-9-13
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|
pubmed:abstractText |
The frontotemporal dementia (FTD) syndromes have been associated with the microtubule-associated tau protein since tau gene mutations have been demonstrated to be the cause of FTD and parkinsonism linked to chromosome 17. In cases of FTD without tau gene mutations, however, it is unclear whether genetic variability in the tau gene is associated with the development or modulation of FTD.
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|
pubmed:language |
eng
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|
pubmed:journal |
|
|
pubmed:citationSubset |
AIM
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|
pubmed:chemical |
|
|
pubmed:status |
MEDLINE
|
|
pubmed:month |
Sep
|
|
pubmed:issn |
0003-9942
|
|
pubmed:author |
|
|
pubmed:issnType |
Print
|
|
pubmed:volume |
62
|
|
pubmed:owner |
NLM
|
|
pubmed:authorsComplete |
Y
|
|
pubmed:pagination |
1419-22
|
|
pubmed:dateRevised |
2009-11-3
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|
pubmed:meshHeading |
pubmed-meshheading:16157749-Age of Onset,
pubmed-meshheading:16157749-Aged,
pubmed-meshheading:16157749-Analysis of Variance,
pubmed-meshheading:16157749-Apolipoproteins E,
pubmed-meshheading:16157749-Case-Control Studies,
pubmed-meshheading:16157749-Chi-Square Distribution,
pubmed-meshheading:16157749-Dementia,
pubmed-meshheading:16157749-Family Health,
pubmed-meshheading:16157749-Female,
pubmed-meshheading:16157749-Genetic Predisposition to Disease,
pubmed-meshheading:16157749-Genotype,
pubmed-meshheading:16157749-Humans,
pubmed-meshheading:16157749-Male,
pubmed-meshheading:16157749-Middle Aged,
pubmed-meshheading:16157749-Retrospective Studies,
pubmed-meshheading:16157749-Sequence Analysis,
pubmed-meshheading:16157749-tau Proteins
|
|
pubmed:year |
2005
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|
pubmed:articleTitle |
Association between tau H2 haplotype and age at onset in frontotemporal dementia.
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|
pubmed:affiliation |
Brain Repair Centre, Department of Clinical Neurosciences, University of Cambridge, England.
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pubmed:publicationType |
Journal Article,
Comparative Study
|
