Source:http://linkedlifedata.com/resource/pubmed/id/15376481
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
2004-9-20
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pubmed:abstractText |
Frontotemporal dementia is a neurodegenerative disease affecting mostly the frontal and/or temporal lobes, with neuronal loss and intraneuronal and/or intraglial inclusions composed of hyperphosphorylated microtubule-associated protein tau and ubiquitin. Missense and splice site mutations in the TAU gene have been identified in approximately 15% of all frontotemporal dementia cases. In this study, we evaluated the involvement of mutations in the TAU gene in development of frontotemporal dementia phenotype in patients of French or English Canadian origins.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Aug
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pubmed:issn |
0317-1671
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
31
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
363-7
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:15376481-Canada,
pubmed-meshheading:15376481-Dementia,
pubmed-meshheading:15376481-Exons,
pubmed-meshheading:15376481-Humans,
pubmed-meshheading:15376481-Mutation,
pubmed-meshheading:15376481-Phenotype,
pubmed-meshheading:15376481-Polymorphism, Genetic,
pubmed-meshheading:15376481-tau Proteins
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pubmed:year |
2004
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pubmed:articleTitle |
TAU mutations are not a predominant cause of frontotemporal dementia in Canadian patients.
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pubmed:affiliation |
Center for Research in Neuroscience, McGill University Health Center Research Institute, Montreal, Quebec, Canada.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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