Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:dateCreated
2007-4-10
pubmed:abstractText
Mutations in the LRRK2 gene have been associated with both familial and sporadic late-onset Parkinson's disease. A large number of mutations in this gene have been identified; however, for many of these variants, the pathogenicity and relative frequency are unknown. Herein, we investigate the frequency of a number of recently identified LRRK2 mutations in Norway.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:issn
0065-1427
pubmed:author
pubmed:issnType
Print
pubmed:volume
187
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
72-5
pubmed:dateRevised
2009-11-19
pubmed:meshHeading
pubmed-meshheading:17419834-Adult, pubmed-meshheading:17419834-Aged, pubmed-meshheading:17419834-Aged, 80 and over, pubmed-meshheading:17419834-Asian Continental Ancestry Group, pubmed-meshheading:17419834-DNA Mutational Analysis, pubmed-meshheading:17419834-Female, pubmed-meshheading:17419834-Gene Frequency, pubmed-meshheading:17419834-Genetic Markers, pubmed-meshheading:17419834-Genetic Predisposition to Disease, pubmed-meshheading:17419834-Genetic Testing, pubmed-meshheading:17419834-Genotype, pubmed-meshheading:17419834-Humans, pubmed-meshheading:17419834-Introns, pubmed-meshheading:17419834-Male, pubmed-meshheading:17419834-Middle Aged, pubmed-meshheading:17419834-Mutation, pubmed-meshheading:17419834-Norway, pubmed-meshheading:17419834-Parkinson Disease, pubmed-meshheading:17419834-Polymorphism, Genetic, pubmed-meshheading:17419834-Protein-Serine-Threonine Kinases
pubmed:year
2007
pubmed:articleTitle
LRRK2 and Parkinson's disease in Norway.
pubmed:affiliation
Department of Neuroscience, Norwegian University of Science and Technology, Trondheim, Norway. mathias.toft@rikshospitalet.no
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't