Clinical features and genetic analysis of a new form of spinocerebellar ataxia

Neurology

Volumn 56, Issue 2, 2001, Pages 234-238

  Devos, D ^a   Schraen Maschke, S ^a   Vuillaume, I ^a   Dujardin, K ^a   Naze P ^a   Willoteaux, C ^a   Destee A ^a   Sablonniere B ^a  

^a LILLE UNIVERSITY HOSPITAL   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; AKINESIA; ARTICLE; ATAXIA; AUTOSOMAL DOMINANT INHERITANCE; CEREBELLUM ATROPHY; CHILD; CLINICAL ARTICLE; CLINICAL FEATURE; DYSARTHRIA; EXTRAPYRAMIDAL SYMPTOM; EYE MOVEMENT; GENE LOCUS; GENE MAPPING; GENE MUTATION; GENE SEQUENCE; GENETIC ANALYSIS; GENETIC HETEROGENEITY; HUMAN; HYPOREFLEXIA; INTELLECTUAL IMPAIRMENT; NUCLEAR MAGNETIC RESONANCE IMAGING; ONSET AGE; PEDIGREE; PHENOTYPE; PRIORITY JOURNAL; SPINOCEREBELLAR DEGENERATION;

EID: 0035936608     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/WNL.56.2.234     Document Type: Article

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