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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
11
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pubmed:dateCreated |
2007-9-11
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pubmed:abstractText |
Spinocerebellar ataxia type 17 (SCA17) is associated with an expansion of CAG/CAA trinucleotide repeats in the gene encoding the TATA-binding protein. In this quantitative characterization of eye movements in SCA17 mutation carriers, we investigated whether eye movement abnormalities originate from multiple lesion sites as suggested by their phenotypic heterogeneity.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
AIM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Sep
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pubmed:issn |
1526-632X
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pubmed:author |
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pubmed:issnType |
Electronic
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pubmed:day |
11
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pubmed:volume |
69
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1160-8
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pubmed:dateRevised |
2009-11-19
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pubmed:meshHeading |
pubmed-meshheading:17846415-Adult,
pubmed-meshheading:17846415-Brain,
pubmed-meshheading:17846415-Cerebellum,
pubmed-meshheading:17846415-DNA Mutational Analysis,
pubmed-meshheading:17846415-Female,
pubmed-meshheading:17846415-Frontal Lobe,
pubmed-meshheading:17846415-Genetic Predisposition to Disease,
pubmed-meshheading:17846415-Genetic Testing,
pubmed-meshheading:17846415-Humans,
pubmed-meshheading:17846415-Male,
pubmed-meshheading:17846415-Middle Aged,
pubmed-meshheading:17846415-Mutation,
pubmed-meshheading:17846415-Neural Pathways,
pubmed-meshheading:17846415-Ocular Motility Disorders,
pubmed-meshheading:17846415-Saccades,
pubmed-meshheading:17846415-Spinocerebellar Ataxias,
pubmed-meshheading:17846415-TATA-Box Binding Protein
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pubmed:year |
2007
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pubmed:articleTitle |
Eye movement abnormalities in spinocerebellar ataxia type 17 (SCA17).
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pubmed:affiliation |
Department of Neurology, University of Luebeck, Luebeck, Germany.
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pubmed:publicationType |
Journal Article
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