Slowly progressive spinocerebellar ataxia with extrapyramidal signs and mild cognitive impairment (SCA21)

Cerebellum

Volumn 7, Issue 2, 2008, Pages 179-183

  Delplanque, J ^a   Devos, D ^b   Vuillaume, I ^b   De Becdelievre, A ^a,b   Vangelder, E ^a   Maurage, C A ^c   Dujardin, K ^b   Destee A ^b   Sablonniere B ^a,b  

^a JEAN PIERRE AUBERT RESEARCH CENTER   (France)

^b UNIV LILLE   (France)

^c LILLE UNIVERSITY HOSPITAL   (France)

Author keywords

Ataxia; Extrapyramidal features; French family; Linkage; Locus; SCA21

Indexed keywords

ADOLESCENT; ADULT; AGED; AKINESIA; ARTICLE; ATAXIA; CHILD; CHROMOSOME 7; DISEASE COURSE; DYSARTHRIA; EXTRAPYRAMIDAL SYMPTOM; FAMILY; FEMALE; FRANCE; GAIT; GENE LOCUS; GENE MAPPING; GENE MUTATION; GENE SEQUENCE; GENETIC ANALYSIS; GENETIC LINKAGE; HUMAN; HUMAN TISSUE; HYPOREFLEXIA; MALE; MILD COGNITIVE IMPAIRMENT; NYSTAGMUS; PATHOGENICITY; POINT MUTATION; PRESCHOOL CHILD; PRIORITY JOURNAL; RIGIDITY; SACCADIC EYE MOVEMENT; SCHOOL CHILD; SPINOCEREBELLAR DEGENERATION; TREMOR; CHROMOSOME MAP; COGNITIVE DEFECT; EXTRAPYRAMIDAL SYNDROME; GENETICS; GENOTYPE; NUCLEOTIDE SEQUENCE; ONSET AGE; PATHOPHYSIOLOGY; PEDIGREE; PHENOTYPE; PSYCHOLOGICAL ASPECT;

ATROPHIN 1; ATROPHIN-1; NERVE PROTEIN;

ADULT; AGE OF ONSET; BASAL GANGLIA DISEASES; CHROMOSOME MAPPING; COGNITION DISORDERS; DISEASE PROGRESSION; DNA MUTATIONAL ANALYSIS; FEMALE; FRANCE; GENOTYPE; HUMANS; LINKAGE (GENETICS); MALE; NERVE TISSUE PROTEINS; PEDIGREE; PHENOTYPE; SPINOCEREBELLAR ATAXIAS; YOUNG ADULT;

EID: 65849478932     PISSN: 14734222     EISSN: 14734230     Source Type: Journal    
DOI: 10.1007/s12311-008-0014-3     Document Type: Article

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