Huntington's disease-like 2: A clinical, pathological, and molecular comparison to Huntington's disease

Clinical Neuroscience Research

Volumn 3, Issue 3, 2003, Pages 187-196

  Margolis, Russell L ^a,b   Holmes, Susan E ^a  

^a Division of Neurobiology   (United States)

^b JOHNS HOPKINS UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

Basal ganglia; Caudate; Huntington's disease; Inclusion; Junctophilin; Neurodegeneration; Striatum; Trinuleotide repeat expansion

Indexed keywords

ADENINE; CYTOSINE; GUANINE; JUNCTOPHILIN 3; POLYGLUTAMINE; PROTEIN; THYMINE; UNCLASSIFIED DRUG;

AUTOSOMAL DOMINANT DISORDER; BRAIN ATROPHY; CELL NUCLEUS INCLUSION BODY; CHROMOSOME 16Q; CLINICAL FEATURE; DEGENERATIVE DISEASE; GENE MUTATION; HUMAN; HUNTINGTON CHOREA; HUNTINGTON DISEASE LIKE 2; MENTAL DISEASE; MOTOR DYSFUNCTION; NEGRO; ONSET AGE; PHENOTYPE; PRIORITY JOURNAL; REVIEW; STRIATE CORTEX; TRINUCLEOTIDE REPEAT;

EID: 0141605228     PISSN: 15662772     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1566-2772(03)00061-6     Document Type: Article

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