Genetics of childhood disorders: X. Huntington disease

Journal of the American Academy of Child and Adolescent Psychiatry

Volumn 39, Issue 1, 2000, Pages 120-122

  DiFiglia, Marian ^a   Lombroso, Paul J ^a,b  

^a MASSACHUSETTS GENERAL HOSPITAL   (United States)

^b YALE UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

GLUTAMINE; HUNTINGTIN; TRINUCLEOTIDE; UBIQUITIN;

ARTICLE; AUTOSOMAL DOMINANT DISORDER; DEGENERATIVE DISEASE; GENE MUTATION; HUMAN; HUNTINGTON CHOREA; NONHUMAN; ONSET AGE; PRIORITY JOURNAL;

EID: 0033981585     PISSN: 08908567     EISSN: None     Source Type: Journal    
DOI: 10.1097/00004583-200001000-00025     Document Type: Article

References (6)

1. M DiFiglia E Sapp KO Chase Aggregation of huntingtin in neuronal intranuclear inclusions and dystrophic neurites in brain Science 277 1997 1990 1993
2. Huntington's Collaborative Research Group A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes Cell 72 1993 971 983
3. M Kim HS Lee G LaForet Mutant huntingtin expression in clonal striatal cells: dissociation of inclusion formation and neuronal survival by caspase inhibition J Neurosci 19 1999 964 973
4. DL Price SS Sisodia DR Borchelt Genetic neurodegenerative diseases: the human illness and transgenic models Science 282 1998 1079 1083
5. JP Vonsattel M DiFiglia Huntington disease J Neuropathol Exp Neurol 57 1998 369 384
6. HW Walling JJ Baldassare TC Westfall Molecular aspects of Huntington's disease J Neurosci Res 54 1998 301 308