TY - JOUR
T1 - Huntington's disease
T2 - A decade beyond gene discovery
AU - Hogarth, Penelope
N1 - Copyright:
Copyright 2018 Elsevier B.V., All rights reserved.
PY - 2003/7
Y1 - 2003/7
N2 - Huntington's disease is a dominantly inherited neurodegenerative disease that causes a progressive movement disorder, cognitive decline, and varying degrees of psychiatric dysfunction. The identification of the mutant gene in 1993 paved the way for a decade of basic research. The resultant advances in our understanding of the pathogenesis of the disorder are moving us toward rational therapies to slow the progression and delay the onset of the illness.
AB - Huntington's disease is a dominantly inherited neurodegenerative disease that causes a progressive movement disorder, cognitive decline, and varying degrees of psychiatric dysfunction. The identification of the mutant gene in 1993 paved the way for a decade of basic research. The resultant advances in our understanding of the pathogenesis of the disorder are moving us toward rational therapies to slow the progression and delay the onset of the illness.
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U2 - 10.1007/s11910-003-0003-3
DO - 10.1007/s11910-003-0003-3
M3 - Review article
C2 - 12930696
AN - SCOPUS:0141610594
SN - 1528-4042
VL - 3
SP - 279
EP - 284
JO - Current Neurology and Neuroscience Reports
JF - Current Neurology and Neuroscience Reports
IS - 4
ER -