The genetic defect causing Huntington's disease: repeated in other contexts?
Mol Med
.
1997 Apr;3(4):238-46.
Authors
J F Gusella
1
,
F Persichetti
,
M E MacDonald
Affiliation
1
Molecular Neurogenetics Unit, Massachusetts General Hospital, Charlestown 02129, USA.
PMID:
9131586
PMCID:
PMC2230063
No abstract available
Publication types
Research Support, Non-U.S. Gov't
Research Support, U.S. Gov't, P.H.S.
Review
MeSH terms
Genotype
Humans
Huntington Disease / genetics*
Phenotype
Trinucleotide Repeats
Grants and funding
NS16367/NS/NINDS NIH HHS/United States
NS32765/NS/NINDS NIH HHS/United States