Autosomal dominant congenital non-progressive ataxia overlaps with the SCA15 locus

Neurology

Volumn 63, Issue 12, 2004, Pages 2288-2292

  Dudding, Tracy E ^a,d   Friend, K ^b   Schofield, P W ^a   Lee, S ^a   Wilkinson, I A ^a   Richards, R I ^c  

^a UNIVERSITY OF NEWCASTLE   (Australia)

^b WOMEN S AND CHILDREN S HOSPITAL   (Australia)

^c UNIVERSITY OF ADELAIDE   (Australia)

^d Hunter Health   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; AGED; ARTICLE; ATAXIA; AUTOSOMAL DOMINANT DISORDER; CEREBELLUM HYPOPLASIA; CHILD; CHROMOSOME 3P; CLINICAL ARTICLE; CLINICAL FEATURE; COGNITIVE DEFECT; DISEASE ASSOCIATION; DYSARTHRIA; DYSDIADOCHOKINESIA; DYSKINESIA; DYSMETRIA; DYSTONIA; FAMILIAL DISEASE; FEMALE; GENE LOCATION; GENE LOCUS; GENETIC RECOMBINATION; GENOME ANALYSIS; HAPLOTYPE; HUMAN; LINKAGE ANALYSIS; MALE; MICROSATELLITE MARKER; MUTATIONAL ANALYSIS; NEUROIMAGING; NONPROGRESSIVE CONGENITAL ATAXIA; NUCLEAR MAGNETIC RESONANCE IMAGING; NYSTAGMUS; PEDIGREE; PRIORITY JOURNAL; PYRAMIDAL SIGN; SCORING SYSTEM; SENSORY DYSFUNCTION; SYMPTOM;

EID: 11144305273     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/01.WNL.0000147299.80872.D1     Document Type: Article

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