Linked Life Data

18314228

Source:http://linkedlifedata.com/resource/pubmed/id/18314228

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
11
pubmed:dateCreated
2009-9-18
pubmed:abstractText
Frontotemporal dementia is a clinically and genetically heterogeneous syndrome. Mutations in two genes, Microtubule Associated Protein Tau (MAPT) and Progranulin (PGRN), and rarely Presenilin mutations, have been causally linked to this disorder.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Nov
pubmed:issn
1558-1497
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
30
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1825-33
pubmed:meshHeading
pubmed:year
2009
pubmed:articleTitle
Novel PSEN1 and PGRN mutations in early-onset familial frontotemporal dementia.
pubmed:affiliation
Regional Neurogenetic Centre, ASP Catanzaro, Lamezia Terme (CZ), Italy.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't