Linked Life Data

21060012

Source:http://linkedlifedata.com/resource/pubmed/id/21060012

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
11
pubmed:dateCreated
2010-11-9
pubmed:abstractText
To determine clinical features and to identify changes in brain structure and function in compound heterozygous and heterozygous ATP13A2 mutation carriers.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
AIM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Nov
pubmed:issn
1538-3687
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
67
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1357-63
pubmed:meshHeading
pubmed-meshheading:21060012-Aged, pubmed-meshheading:21060012-Brain, pubmed-meshheading:21060012-Brain Mapping, pubmed-meshheading:21060012-Color Perception, pubmed-meshheading:21060012-Discrimination (Psychology), pubmed-meshheading:21060012-Female, pubmed-meshheading:21060012-Genetic Predisposition to Disease, pubmed-meshheading:21060012-Heterozygote, pubmed-meshheading:21060012-Humans, pubmed-meshheading:21060012-Magnetic Resonance Imaging, pubmed-meshheading:21060012-Male, pubmed-meshheading:21060012-Middle Aged, pubmed-meshheading:21060012-Mutation, pubmed-meshheading:21060012-Nerve Degeneration, pubmed-meshheading:21060012-Olfactory Perception, pubmed-meshheading:21060012-Parkinsonian Disorders, pubmed-meshheading:21060012-Pedigree, pubmed-meshheading:21060012-Phenotype, pubmed-meshheading:21060012-Prospective Studies, pubmed-meshheading:21060012-Proton-Translocating ATPases
pubmed:year
2010
pubmed:articleTitle
Recessively inherited parkinsonism: effect of ATP13A2 mutations on the clinical and neuroimaging phenotype.
pubmed:affiliation
Schilling Section of Clinical and Molecular Neurogenetics and Department of Neurology, University of Lübeck, Ratzeburger Allee 160, 23538 Lübeck, Germany.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't