17662000

Source:http://linkedlifedata.com/resource/pubmed/id/17662000

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0026882, umls-concept:C0205314, umls-concept:C0241888, umls-concept:C0332281, umls-concept:C0338451, umls-concept:C0679622, umls-concept:C1446659
pubmed:issue	8
pubmed:dateCreated	2007-7-30
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/9506311
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Codon, http://linkedlifedata.com/resource/pubmed/chemical/tau Proteins
pubmed:status	MEDLINE
pubmed:month	Aug
pubmed:issn	1468-1331
pubmed:author	pubmed-author:EzquerraMM, pubmed-author:LlahiSS, pubmed-author:MolinuevoJ LJL, pubmed-author:RambCC, pubmed-author:Sánchez-ValleRR, pubmed-author:TolosaEE
pubmed:issnType	Electronic
pubmed:volume	14
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	e9-10
pubmed:meshHeading	pubmed-meshheading:17662000-Akinetic Mutism, pubmed-meshheading:17662000-Base Sequence, pubmed-meshheading:17662000-Brain, pubmed-meshheading:17662000-Codon, pubmed-meshheading:17662000-Cognition Disorders, pubmed-meshheading:17662000-DNA Mutational Analysis, pubmed-meshheading:17662000-Dementia, pubmed-meshheading:17662000-Family Health, pubmed-meshheading:17662000-Female, pubmed-meshheading:17662000-Gait Disorders, Neurologic, pubmed-meshheading:17662000-Genetic Predisposition to Disease, pubmed-meshheading:17662000-Humans, pubmed-meshheading:17662000-Male, pubmed-meshheading:17662000-Middle Aged, pubmed-meshheading:17662000-Mutation, pubmed-meshheading:17662000-Pedigree, pubmed-meshheading:17662000-Point Mutation, pubmed-meshheading:17662000-Spain, pubmed-meshheading:17662000-tau Proteins
pubmed:year	2007
pubmed:articleTitle	A novel MAPT mutation (P301T) associated with familial frontotemporal dementia.
pubmed:publicationType	Letter, Case Reports, Research Support, Non-U.S. Gov't