20142525

Source:http://linkedlifedata.com/resource/pubmed/id/20142525

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0026882, umls-concept:C0031437, umls-concept:C0332281, umls-concept:C1415311
pubmed:issue	2
pubmed:dateCreated	2010-2-9
pubmed:abstractText	To characterize a kindred with a familial neurodegenerative disorder associated with a mutation in progranulin (PGRN), with emphasis on the unique clinical features in this kindred.
pubmed:grant	http://linkedlifedata.com/resource/pubmed/grant/AG06786, http://linkedlifedata.com/resource/pubmed/grant/AG07216, http://linkedlifedata.com/resource/pubmed/grant/AG11378, http://linkedlifedata.com/resource/pubmed/grant/AG16574, http://linkedlifedata.com/resource/pubmed/grant/P50 AG016574-07, http://linkedlifedata.com/resource/pubmed/grant/R01 AG011378-15, http://linkedlifedata.com/resource/pubmed/grant/U01 AG006786-22
pubmed:commentsCorrections	http://linkedlifedata.com/resource/pubmed/commentcorrection/20142525-10219785, http://linkedlifedata.com/resource/pubmed/commentcorrection/20142525-11571213, http://linkedlifedata.com/resource/pubmed/commentcorrection/20142525-11708987, http://linkedlifedata.com/resource/pubmed/commentcorrection/20142525-12056930, http://linkedlifedata.com/resource/pubmed/commentcorrection/20142525-15324362, http://linkedlifedata.com/resource/pubmed/commentcorrection/20142525-15615814, http://linkedlifedata.com/resource/pubmed/commentcorrection/20142525-16401619, http://linkedlifedata.com/resource/pubmed/commentcorrection/20142525-16606762, http://linkedlifedata.com/resource/pubmed/commentcorrection/20142525-16783167, http://linkedlifedata.com/resource/pubmed/commentcorrection/20142525-16862116, http://linkedlifedata.com/resource/pubmed/commentcorrection/20142525-16950801, http://linkedlifedata.com/resource/pubmed/commentcorrection/20142525-16983685, http://linkedlifedata.com/resource/pubmed/commentcorrection/20142525-17023659, http://linkedlifedata.com/resource/pubmed/commentcorrection/20142525-17030534, http://linkedlifedata.com/resource/pubmed/commentcorrection/20142525-17030535, http://linkedlifedata.com/resource/pubmed/commentcorrection/20142525-17210807, http://linkedlifedata.com/resource/pubmed/commentcorrection/20142525-17278999, http://linkedlifedata.com/resource/pubmed/commentcorrection/20142525-17353379, http://linkedlifedata.com/resource/pubmed/commentcorrection/20142525-3561043, http://linkedlifedata.com/resource/pubmed/commentcorrection/20142525-9152110, http://linkedlifedata.com/resource/pubmed/commentcorrection/20142525-9641683, http://linkedlifedata.com/resource/pubmed/commentcorrection/20142525-9855500
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0372436
pubmed:citationSubset	AIM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/GRN protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Intercellular Signaling Peptides...
pubmed:status	MEDLINE
pubmed:month	Feb
pubmed:issn	1538-3687
pubmed:author	pubmed-author:AdamsonJenniferJ, pubmed-author:BakerMattM, pubmed-author:BoeveBradley FBF, pubmed-author:DicksonDennis WDW, pubmed-author:HaidarWaelW, pubmed-author:HuttonMikeM, pubmed-author:KelleyBrendan JBJ, pubmed-author:KnopmanDavid SDS, pubmed-author:KuntzKaren MKM, pubmed-author:ParisiJoseph EJE, pubmed-author:PetersenRonald CRC, pubmed-author:RademakersRosaR, pubmed-author:ShiungMariaM, pubmed-author:SmithGlenn EGE
pubmed:issnType	Electronic
pubmed:volume	67
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	171-7
pubmed:dateRevised	2011-7-22
pubmed:meshHeading	pubmed-meshheading:20142525-Aged, pubmed-meshheading:20142525-Aged, 80 and over, pubmed-meshheading:20142525-Alzheimer Disease, pubmed-meshheading:20142525-Cognition Disorders, pubmed-meshheading:20142525-Family Health, pubmed-meshheading:20142525-Female, pubmed-meshheading:20142525-Gene Deletion, pubmed-meshheading:20142525-Genetic Association Studies, pubmed-meshheading:20142525-Genetic Predisposition to Disease, pubmed-meshheading:20142525-Genotype, pubmed-meshheading:20142525-Humans, pubmed-meshheading:20142525-Intercellular Signaling Peptides and Proteins, pubmed-meshheading:20142525-Magnetic Resonance Imaging, pubmed-meshheading:20142525-Male, pubmed-meshheading:20142525-Middle Aged, pubmed-meshheading:20142525-Neuropsychological Tests, pubmed-meshheading:20142525-Phenotype
pubmed:year	2010
pubmed:articleTitle	Alzheimer disease-like phenotype associated with the c.154delA mutation in progranulin.
pubmed:affiliation	Department of Neurology, Mayo Clinic, 200 First Street SW, Rochester, MN 55905, USA.
pubmed:publicationType	Journal Article, Research Support, Non-U.S. Gov't, Research Support, N.I.H., Extramural