Linked Life Data

17353388

Source:http://linkedlifedata.com/resource/pubmed/id/17353388

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
3
pubmed:dateCreated
2007-3-13
pubmed:abstractText
Mutations in leucine-rich repeat kinase 2 gene (LRRK2), particularly the G2019S mutation in exon 41, have been detected in familial and sporadic Parkinson disease (PD) cases.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
AIM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Mar
pubmed:issn
0003-9942
pubmed:author
pubmed-author:AgidYvesY, pubmed-author:BonnetAnne-MarieAM, pubmed-author:BorgMichelM, pubmed-author:BriceAlexisA, pubmed-author:BroussolleEmmanuelE, pubmed-author:DürrAlexandraA, pubmed-author:DamierPhilippeP, pubmed-author:DestéeAlainA, pubmed-author:DurifFranckF, pubmed-author:French Parkinson's Disease Genetics Study Group, pubmed-author:JaninSabineS, pubmed-author:LayetValérieV, pubmed-author:LeclereLaurenceL, pubmed-author:LesageSuzanneS, pubmed-author:LeuteneggerAnne-LouiseAL, pubmed-author:LohmannEbbaE, pubmed-author:MartinezMariaM, pubmed-author:PenetChristianeC, pubmed-author:PollakPierreP, pubmed-author:RascoOlivierO, pubmed-author:ThoboisStéphaneS, pubmed-author:TisonFrançoisF, pubmed-author:TranchanChristineC, pubmed-author:VérinMarcM, pubmed-author:VialletFrançoisF, pubmed-author:VidailhetMarieM
pubmed:issnType
Print
pubmed:volume
64
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
425-30
pubmed:dateRevised
2007-11-15
pubmed:meshHeading
pubmed:year
2007
pubmed:articleTitle
LRRK2 exon 41 mutations in sporadic Parkinson disease in Europeans.
pubmed:affiliation
Institut National de la Santé et de la Recherche Médicale Unité 679, Neurology and Experimental Therapeutics, and Faculté de Médecine, Université Pierre et Marie Curie, 75651 Paris CEDEX 13, France.
pubmed:publicationType
Journal Article, Comparative Study, Research Support, Non-U.S. Gov't, Research Support, N.I.H., Extramural