Molecular and clinical findings in a family with dentatorubral‐pallidoluysian atrophy

Annals of Neurology

Volumn 37, Issue 2, 1995, Pages 273-277

  Potter, Nicholas T ^a,b   Meyer, Michael A ^a   Zimmerman, Andrew W ^b,c   Eisenstadt, Michael L ^c   Anderson, Ilse J ^a,b  

^a UNIVERSITY OF TENNESSEE   (United States)

^b UNIVERSITY OF TENNESSEE MEDICAL CENTER   (United States)

^c Knoxville Neurology Clinic   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; ATAXIA; AUTOSOMAL DOMINANT DISORDER; CASE REPORT; CLINICAL FEATURE; DEMENTIA; DENTATORUBROPALLIDOLUYSIAN ATROPHY; FEMALE; GENE MUTATION; HUMAN; HUNTINGTON CHOREA; HYPOTHESIS; MALE; MENTAL DEFICIENCY; MENTAL DISEASE; NERVE DEGENERATION; NUCLEAR MAGNETIC RESONANCE IMAGING; PRIORITY JOURNAL; SEIZURE; WHITE MATTER;

ADOLESCENT; ADULT; ATHETOSIS; CHOREA; EPILEPSIES, MYOCLONIC; FEMALE; HUMAN; MAGNETIC RESONANCE IMAGING; MALE; MIDDLE AGE; MUTATION; PEDIGREE; SUPPORT, NON-U.S. GOV'T; SYNDROME;

EID: 0028797080     PISSN: 03645134     EISSN: 15318249     Source Type: Journal    
DOI: 10.1002/ana.410370220     Document Type: Article

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