17620546

Source:http://linkedlifedata.com/resource/pubmed/id/17620546

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0019409, umls-concept:C0026882, umls-concept:C0205314, umls-concept:C0338451, umls-concept:C0598429, umls-concept:C0679622, umls-concept:C1415311
pubmed:issue	2
pubmed:dateCreated	2007-7-10
pubmed:abstractText	Frontotemporal dementia (FTD) in several 17q21-linked families was recently explained by truncating mutations in the progranulin gene (GRN).
pubmed:commentsCorrections	http://linkedlifedata.com/resource/pubmed/commentcorrection/17620546-17620543
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0401060
pubmed:citationSubset	AIM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/GRN protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Genetic Markers, http://linkedlifedata.com/resource/pubmed/chemical/Intercellular Signaling Peptides...
pubmed:status	MEDLINE
pubmed:month	Jul
pubmed:issn	1526-632X
pubmed:author	pubmed-author:AnfossiMM, pubmed-author:BernardiLL, pubmed-author:BruniA CAC, pubmed-author:ColasNN, pubmed-author:CostanziGG, pubmed-author:CurcioS A MSA, pubmed-author:ElderJJ, pubmed-author:FrangipaneFF, pubmed-author:GalloMM, pubmed-author:GeracitanoSS, pubmed-author:HardyJJ, pubmed-author:KawaraiTT, pubmed-author:KerteszAA, pubmed-author:MalettaR GRG, pubmed-author:MirabelliMM, pubmed-author:MomeniPP, pubmed-author:PradellaSS, pubmed-author:PuccioGG, pubmed-author:RogaevaEE, pubmed-author:SatoCC, pubmed-author:SmirneNN, pubmed-author:St George-HyslopPP, pubmed-author:TomainoCC, pubmed-author:WakutaniYY
pubmed:issnType	Electronic
pubmed:day	10
pubmed:volume	69
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	140-7
pubmed:dateRevised	2009-11-19
pubmed:meshHeading	pubmed-meshheading:17620546-Adult, pubmed-meshheading:17620546-Age of Onset, pubmed-meshheading:17620546-Aged, pubmed-meshheading:17620546-Aged, 80 and over, pubmed-meshheading:17620546-Chromosomes, Human, Pair 17, pubmed-meshheading:17620546-Cohort Studies, pubmed-meshheading:17620546-DNA Mutational Analysis, pubmed-meshheading:17620546-Dementia, pubmed-meshheading:17620546-Female, pubmed-meshheading:17620546-Gene Frequency, pubmed-meshheading:17620546-Genetic Markers, pubmed-meshheading:17620546-Genetic Predisposition to Disease, pubmed-meshheading:17620546-Genetic Testing, pubmed-meshheading:17620546-Genotype, pubmed-meshheading:17620546-Heterozygote, pubmed-meshheading:17620546-Heterozygote Detection, pubmed-meshheading:17620546-Humans, pubmed-meshheading:17620546-Intercellular Signaling Peptides and Proteins, pubmed-meshheading:17620546-Italy, pubmed-meshheading:17620546-Male, pubmed-meshheading:17620546-Middle Aged, pubmed-meshheading:17620546-Mutation, pubmed-meshheading:17620546-Pedigree
pubmed:year	2007
pubmed:articleTitle	Heterogeneity within a large kindred with frontotemporal dementia: a novel progranulin mutation.
pubmed:affiliation	Regional Neurogenetic Centre, Lamezia Terme, CZ, Italy. bruni@arn.it
pubmed:publicationType	Journal Article, Research Support, Non-U.S. Gov't, Research Support, N.I.H., Intramural