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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
3
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pubmed:dateCreated |
2006-9-25
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pubmed:abstractText |
Mutations in the Progranulin gene (PGRN) recently have been discovered to be associated with frontotemporal dementia (FTD) linked to 17q21 without identified MAPT mutations. The range of mutations of PGRN that can result in the FTD phenotype and the clinical presentation of patients with PGRN mutations have yet to be determined.
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pubmed:grant |
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Sep
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pubmed:issn |
0364-5134
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pubmed:author |
pubmed-author:BakerMattM,
pubmed-author:BergerStephen LSL,
pubmed-author:ElderJoshua WJW,
pubmed-author:GhettiBernardinoB,
pubmed-author:GrafmanJordanJ,
pubmed-author:HardyJohnJ,
pubmed-author:HeflinKyle AKA,
pubmed-author:HueyEdward DED,
pubmed-author:HuttonMikeM,
pubmed-author:MomeniParastooP,
pubmed-author:PietriniPietroP,
pubmed-author:SpinaSalvatoreS,
pubmed-author:TierneyMichael CMC,
pubmed-author:WassermannEric MEM
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pubmed:issnType |
Print
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pubmed:volume |
60
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
374-80
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pubmed:dateRevised |
2011-9-29
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pubmed:meshHeading |
pubmed-meshheading:16983677-Adolescent,
pubmed-meshheading:16983677-Adult,
pubmed-meshheading:16983677-Age of Onset,
pubmed-meshheading:16983677-Aged,
pubmed-meshheading:16983677-Aged, 80 and over,
pubmed-meshheading:16983677-Arginine,
pubmed-meshheading:16983677-Chromosomes, Human, Pair 17,
pubmed-meshheading:16983677-DNA Mutational Analysis,
pubmed-meshheading:16983677-Dementia,
pubmed-meshheading:16983677-Deoxyglucose,
pubmed-meshheading:16983677-Female,
pubmed-meshheading:16983677-Gene Frequency,
pubmed-meshheading:16983677-Genetic Predisposition to Disease,
pubmed-meshheading:16983677-Humans,
pubmed-meshheading:16983677-Intercellular Signaling Peptides and Proteins,
pubmed-meshheading:16983677-Male,
pubmed-meshheading:16983677-Microtubule-Associated Proteins,
pubmed-meshheading:16983677-Middle Aged,
pubmed-meshheading:16983677-Mutation,
pubmed-meshheading:16983677-Neuropsychological Tests,
pubmed-meshheading:16983677-Positron-Emission Tomography,
pubmed-meshheading:16983677-tau Proteins
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pubmed:year |
2006
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pubmed:articleTitle |
Characteristics of frontotemporal dementia patients with a Progranulin mutation.
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pubmed:affiliation |
Cognitive Neuroscience Section, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD 20892-1440, USA.
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pubmed:publicationType |
Journal Article,
Comparative Study,
Research Support, Non-U.S. Gov't,
Research Support, N.I.H., Extramural
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