Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
7
pubmed:dateCreated
2007-7-10
pubmed:abstractText
Individuals with fragile X-associated tremor/ataxia syndrome frequently have associated features of parkinsonism, often leading to an initial diagnosis of Parkinson disease or other parkinsonism spectrum disorders. Parkinson disease populations may thus include individuals who harbor premutation expansions (55-200 CGG repeats) of the fragile X mental retardation 1 (FMR1) gene.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
AIM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jul
pubmed:issn
0003-9942
pubmed:author
pubmed:issnType
Print
pubmed:volume
64
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1002-6
pubmed:dateRevised
2009-11-19
pubmed:meshHeading
pubmed-meshheading:17620491-Aged, pubmed-meshheading:17620491-Alleles, pubmed-meshheading:17620491-Cohort Studies, pubmed-meshheading:17620491-DNA Mutational Analysis, pubmed-meshheading:17620491-DNA Repeat Expansion, pubmed-meshheading:17620491-Fragile X Mental Retardation Protein, pubmed-meshheading:17620491-Fragile X Syndrome, pubmed-meshheading:17620491-Gene Frequency, pubmed-meshheading:17620491-Genetic Markers, pubmed-meshheading:17620491-Genetic Predisposition to Disease, pubmed-meshheading:17620491-Genetic Testing, pubmed-meshheading:17620491-Genotype, pubmed-meshheading:17620491-Heterozygote, pubmed-meshheading:17620491-Humans, pubmed-meshheading:17620491-Male, pubmed-meshheading:17620491-Middle Aged, pubmed-meshheading:17620491-Mutation, pubmed-meshheading:17620491-Parkinson Disease, pubmed-meshheading:17620491-Phenotype, pubmed-meshheading:17620491-Sex Factors
pubmed:year
2007
pubmed:articleTitle
Screen for excess FMR1 premutation alleles among males with parkinsonism.
pubmed:affiliation
Department of Biochemistry and Molecular Medicine, University of California, Davis, School of Medicine, One Shields Avenue, Davis, CA 95616, USA.
pubmed:publicationType
Journal Article, Case Reports, Research Support, Non-U.S. Gov't