Autosomal dominant cerebellar ataxia type III: a review of the phenotypic and genotypic characteristics.

Orphanet journal of rare diseases

Volumn 8, Issue , 2013, Pages

  Fujioka, Shinsuke ^a   Sundal, Christina ^b   Wszolek, Zbigniew K ^b  

^a MAYO CLINIC   (United States)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

CLASSIFICATION; DIFFERENTIAL DIAGNOSIS; EXERCISE; GENETICS; GENOTYPE; HUMAN; MUTATION; PATHOPHYSIOLOGY; PHENOTYPE; PREVALENCE; REVIEW; SPINOCEREBELLAR DEGENERATION; TRINUCLEOTIDE REPEAT;

DIAGNOSIS, DIFFERENTIAL; EXERCISE; GENOTYPE; HUMANS; MUTATION; PHENOTYPE; PREVALENCE; SPINOCEREBELLAR ATAXIAS; TRINUCLEOTIDE REPEATS;

EID: 84872351419     PISSN: None     EISSN: 17501172     Source Type: None    
DOI: 10.1186/1750-1172-8-14     Document Type: Review

References (0)