Eye movement abnormalities in spinocerebellar ataxia type 17 (SCA17)

Neurology

Volumn 69, Issue 11, 2007, Pages 1160-1168

  Hubner J ^a   Sprenger, A ^a   Klein, C ^a   Hagenah, J ^a   Rambold, H ^a,b   Zuhlke C ^a   Kompf D ^a   Rolfs, A ^c   Kimmig, H ^a   Helmchen, C ^a  

^a UNIVERSITY OF LÜBECK   (Germany)

^b NATIONAL EYE INSTITUTE   (United States)

^c UNIVERSITY OF ROSTOCK   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

TATA BINDING PROTEIN;

ADULT; ARTICLE; CLINICAL ARTICLE; CONTROLLED STUDY; DEMENTIA; DISEASE DURATION; EYE MOVEMENT DISORDER; FEMALE; GENE MUTATION; HUMAN; LATENT PERIOD; MALE; PARKINSONISM; PHENOTYPE; PRIORITY JOURNAL; REFLEX; SACCADIC EYE MOVEMENT; SMOOTH PURSUIT EYE MOVEMENT; SPINOCEREBELLAR DEGENERATION; VISUAL MEMORY;

ADULT; BRAIN; CEREBELLUM; DNA MUTATIONAL ANALYSIS; FEMALE; FRONTAL LOBE; GENETIC PREDISPOSITION TO DISEASE; GENETIC SCREENING; HUMANS; MALE; MIDDLE AGED; MUTATION; NEURAL PATHWAYS; OCULAR MOTILITY DISORDERS; SACCADES; SPINOCEREBELLAR ATAXIAS; TATA-BOX BINDING PROTEIN;

EID: 34948839850     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/01.wnl.0000276958.91986.89     Document Type: Article

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