Intrafamilial variability of Parkinson phenotype in SCAs: Novel cases due to SCA2 and SCA3 expansions

Parkinsonism and Related Disorders

Volumn 15, Issue 5, 2009, Pages 374-378

  Socal, M P ^a   Emmel, V E ^a   Rieder, C R M ^a,b   Hilbig, A ^c   Saraiva Pereira, M L ^a,b   Jardim, L B ^a,b  

^a FEDERAL UNIVERSITY OF RIO GRANDE DO SUL   (Brazil)

^b HOSPITAL DE CLÍNICAS DE PORTO ALEGRE   (Brazil)

^c UNIVERSIDADE FEDERAL DE CIÊNCIAS DA SAÚDE DE PORTO ALEGRE   (Brazil)

Author keywords

Dominant inheritance; Parkinson's disease; SCA2; SCA3; Spinocerebellar ataxia

Indexed keywords

ATAXIN 1; LEVODOPA;

ADULT; AGED; ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; BRAZIL; CLINICAL FEATURE; DISEASE DURATION; ETHNICITY; FAMILY HISTORY; FAMILY STUDY; FEMALE; GENE MUTATION; GEOGRAPHIC ORIGIN; HUMAN; MAJOR CLINICAL STUDY; MALE; NEUROLOGIC EXAMINATION; ONSET AGE; PARKINSON DISEASE; PEDIGREE; PHENOTYPE; PRIORITY JOURNAL; SPINOCEREBELLAR DEGENERATION;

ADULT; AGE OF ONSET; ANTIPARKINSON AGENTS; DNA REPEAT EXPANSION; FAMILY; FEMALE; GENES, DOMINANT; GENETIC VARIATION; HUMANS; LEVODOPA; MACHADO-JOSEPH DISEASE; MALE; MIDDLE AGED; NERVE TISSUE PROTEINS; NUCLEAR PROTEINS; PARKINSON DISEASE; PEDIGREE; PHENOTYPE; REPRESSOR PROTEINS; SPINOCEREBELLAR DEGENERATIONS;

EID: 67349277693     PISSN: 13538020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.parkreldis.2008.09.005     Document Type: Article

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