Clinical phenotype of Brazilian families with spinocerebellar ataxia 10

Neurology

Volumn 63, Issue 8, 2004, Pages 1509-1512

  Teive, H A G ^a   Roa, B B ^c   Raskin, S ^a   Fang, P ^c   Arruda, W O ^a   Neto, Y Correa ^b   Gao, R ^d   Werneck, L C ^a   Ashizawa, Tetsuo ^d  

^a FEDERAL UNIVERSITY OF PARANÁ   (Brazil)

^b Hospital Universitario   (Brazil)

^c BAYLOR COLLEGE OF MEDICINE   (United States)

^d University of Texas Medical Branch School of Medicine   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DNA;

ADULT; ARTICLE; AUTOSOMAL DOMINANT DISORDER; BRAZIL; CEREBELLAR ATAXIA; CLINICAL ARTICLE; CLINICAL FEATURE; COMPUTER ASSISTED TOMOGRAPHY; DNA DETERMINATION; ELECTROMYOGRAM; EPILEPSY; FEMALE; GENE; GENE MUTATION; HUMAN; INTRON; MALE; MEXICO; NEUROPSYCHOLOGICAL TEST; NUCLEAR MAGNETIC RESONANCE IMAGING; NUCLEOTIDE REPEAT; PHENOTYPE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SCA10 GENE; SPINOCEREBELLAR DEGENERATION;

EID: 7044274091     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/01.WNL.0000142109.62056.57     Document Type: Article

References (10)

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