Atypical Parkinsonism and SCA8

Parkinsonism and Related Disorders

Volumn 12, Issue 6, 2006, Pages 396-

  Baba, Yasuhiko ^a   Uitti, Ryan J ^a   Farrer, Matthew J ^a   Wszolek, Zbigniew K ^a  

^a MAYO CLINIC   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

POLYLYSINE; PROTEIN; SCA 8 PROTEIN; UNCLASSIFIED DRUG;

CEREBELLUM ATROPHY; CORTICOBASAL DEGENERATION; GENE LOCUS; GENETIC COUNSELING; GENETIC SUSCEPTIBILITY; GENOTYPE PHENOTYPE CORRELATION; HUMAN; LETTER; PARKINSONISM; PATIENT; PRIORITY JOURNAL;

HUMANS; NERVE TISSUE PROTEINS; PARKINSONIAN DISORDERS; TRINUCLEOTIDE REPEAT EXPANSION;

EID: 33746896173     PISSN: 13538020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.parkreldis.2006.06.001     Document Type: Letter

References (2)

1. Baba Y., Uitti R.J., Farrer M.J., and Wszolek Z.K. Sporadic SCA8 mutation resembling corticobasal degeneration. Parkinsonism Relat Disord 11 (2005) 147-150
2. Factor S.A., Qian J., Lava N.S., Hubbard J.D., and Payami H. False-positive SCA8 gene test in a patient with pathologically proven multiple system atrophy. Ann Neurol 57 (2005) 462-463