16966502

Source:http://linkedlifedata.com/resource/pubmed/id/16966502

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0019904, umls-concept:C0026882, umls-concept:C0030567, umls-concept:C0030705, umls-concept:C0205210, umls-concept:C1425650, umls-concept:C2348519
pubmed:issue	9
pubmed:dateCreated	2006-9-12
pubmed:abstractText	The G2019S mutation is the most common pathogenic substitution in the leucine-rich repeat kinase 2 (LRRK2) gene, which has recently been identified in familial and sporadic Parkinson disease (PD).
pubmed:grant	http://linkedlifedata.com/resource/pubmed/grant/K08 NS 044138, http://linkedlifedata.com/resource/pubmed/grant/NS 41723-01A1, http://linkedlifedata.com/resource/pubmed/grant/P50 NS 40256-02, http://linkedlifedata.com/resource/pubmed/grant/R01 NS 037167
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0372436
pubmed:citationSubset	AIM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Glycine, http://linkedlifedata.com/resource/pubmed/chemical/LRRK2 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Protein-Serine-Threonine Kinases, http://linkedlifedata.com/resource/pubmed/chemical/Serine
pubmed:status	MEDLINE
pubmed:month	Sep
pubmed:issn	0003-9942
pubmed:author	pubmed-author:AmouriRimR, pubmed-author:BriceAlexisA, pubmed-author:DürrAlexandraA, pubmed-author:FarrerMatthew JMJ, pubmed-author:ForoudTatiana MTM, pubmed-author:GibsonRachelR, pubmed-author:GriffithAlidaA, pubmed-author:HattoriNobutakaN, pubmed-author:HentatiFaycalF, pubmed-author:IshiharaLiannaL, pubmed-author:LeppertDavidD, pubmed-author:LesageSuzanneS, pubmed-author:MiddletonLefkosL, pubmed-author:NicholsWilliam CWC, pubmed-author:TazirMeriemM, pubmed-author:UittiRyan JRJ, pubmed-author:WarrenLilingL, pubmed-author:WattsRayR, pubmed-author:WszolekZbigniew KZK, pubmed-author:ZabetianCyrus PCP
pubmed:issnType	Print
pubmed:volume	63
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	1250-4
pubmed:dateRevised	2009-11-3
pubmed:meshHeading	pubmed-meshheading:16966502-Aged, pubmed-meshheading:16966502-DNA Mutational Analysis, pubmed-meshheading:16966502-Family Health, pubmed-meshheading:16966502-Female, pubmed-meshheading:16966502-Gene Frequency, pubmed-meshheading:16966502-Genetic Predisposition to Disease, pubmed-meshheading:16966502-Glycine, pubmed-meshheading:16966502-Humans, pubmed-meshheading:16966502-Male, pubmed-meshheading:16966502-Middle Aged, pubmed-meshheading:16966502-Mutation, pubmed-meshheading:16966502-Parkinson Disease, pubmed-meshheading:16966502-Protein-Serine-Threonine Kinases, pubmed-meshheading:16966502-Serine
pubmed:year	2006
pubmed:articleTitle	Clinical features of Parkinson disease patients with homozygous leucine-rich repeat kinase 2 G2019S mutations.
pubmed:affiliation	Department of Public Health and Primary Care, University of Cambridge, Cambridge, England.
pubmed:publicationType	Journal Article, Comparative Study, Research Support, U.S. Gov't, Non-P.H.S., Research Support, Non-U.S. Gov't, Research Support, N.I.H., Extramural