Autosomal dominant cerebellar ataxia type I. Clinical features and MRI in families with SCA1, SCA2 and SCA3

Brain

Volumn 119, Issue 5, 1996, Pages 1497-1505

  Burk K ^a   Abele, M ^a   Fetter, M ^a   Dichgans, J ^a   Skalej, M ^a   Laccone, F ^b   Didierjean, O ^c   Brice, A ^c   Klockgether, T ^a  

^a UNIVERSITY OF TÜBINGEN   (Germany)

^b UNIVERSITY OF GÖTTINGEN   (Germany)

^c PITIÉ SALPÊTRIÈRE HOSPITAL   (France)

Author keywords

Autosomal dominant cerebellar ataxia; Saccade velocity; Trinucleotide repeat

Indexed keywords

ARTICLE; AUTOSOMAL DOMINANT DISORDER; BRAIN STEM; CEREBELLAR ATAXIA; CLINICAL FEATURE; DIAGNOSTIC TEST; DYSPHAGIA; EYE MOVEMENT; GENETIC HETEROGENEITY; GENOTYPE; HUMAN; MAJOR CLINICAL STUDY; MORPHOMETRICS; NUCLEAR MAGNETIC RESONANCE IMAGING; OLIVOPONTOCEREBELLAR ATROPHY; PHENOTYPE; PRIORITY JOURNAL; PYRAMIDAL TRACT; SACCADIC EYE MOVEMENT;

EID: 0029959667     PISSN: 00068950     EISSN: None     Source Type: Journal    
DOI: 10.1093/brain/119.5.1497     Document Type: Article

References (42)

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