The unique co-occurrence of spinocerebellar ataxia type 10 (SCA10) and Huntington disease

Journal of the Neurological Sciences

Volumn 324, Issue 1-2, 2013, Pages 176-178

  Roxburgh, Richard H ^a,b   Smith, Corrie O ^c   Lim, Jung G ^d   Bachman, David F ^e   Byrd, Erica ^c   Bird, Thomas D ^c,f  

^a AUCKLAND CITY HOSPITAL   (New Zealand)

^b UNIVERSITY OF AUCKLAND   (New Zealand)

^c UNIVERSITY OF WASHINGTON   (United States)

^d Lourdes Medical Center   (United States)

^e VA Puget Sound Health Care System ^*  (United States)

^f VA PUGET SOUND HEALTH CARE SYSTEM   (United States)

Author keywords

Huntington disease; Neurogenetics; Spinocerebellar ataxia; Trinucleotide repeat

Indexed keywords

PROTEIN; SPINOCEREBELLAR ATAXIA TYPE 10 PROTEIN; UNCLASSIFIED DRUG;

ADULT; AMERICAN INDIAN; ARTICLE; CAG REPEAT; CASE REPORT; CEREBELLUM ATROPHY; COGNITION; DYSARTHRIA; DYSTONIA; FEMALE; HUMAN; HUNTINGTON CHOREA; NUCLEAR MAGNETIC RESONANCE IMAGING; ONSET AGE; PATHOGENESIS; PHENOTYPE; PRIORITY JOURNAL;

EID: 84870956362     PISSN: 0022510X     EISSN: 18785883     Source Type: Journal    
DOI: 10.1016/j.jns.2012.09.030     Document Type: Article

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