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Journal Article
Lancet Neurology, The, ISSN 1474-4422, 2011, Volume 10, Issue 1, pp. 31 - 42
Journal Article
Lancet Neurology, The, ISSN 1474-4422, 2012, Volume 11, Issue 1, pp. 42 - 53
Journal Article
Neurology, ISSN 0028-3878, 03/2012, Volume 78, Issue 10, pp. 690 - 695
Objective: Age at onset of diagnostic motor manifestations in Huntington disease (HD) is strongly correlated with an expanded CAG trinucleotide repeat. The... 
HOMOZYGOSITY | ALLELE | OF-ONSET | GENE | LENGTH | MUTATION | CHROMOSOMES | CLINICAL NEUROLOGY | TRINUCLEOTIDE REPEAT | Humans | Age of Onset | Alleles | Huntington Disease - genetics | Adult | Female | Genotype | Huntington Disease - diagnosis | Male | Trinucleotide Repeat Expansion | 164
Journal Article
Nature Reviews Neurology, ISSN 1759-4758, 2014, Volume 10, Issue 4, pp. 204 - 216
Huntington disease (HD) can be seen as a model neurodegenerative disorder, in that it is caused by a single genetic mutation and is amenable to predictive... 
COGNITIVE DYSFUNCTION | METABOLIC NETWORK | BASAL GANGLIA VOLUME | FUNCTIONAL CONNECTIVITY | CAG-REPEAT LENGTH | CEREBROSPINAL-FLUID | WHITE-MATTER VOLUME | PRE-MANIFEST | CLINICAL PROGRESSION | CLINICAL NEUROLOGY | AGE-OF-ONSET | Development and progression | Care and treatment | Diagnosis | Huntington's chorea | Genetic screening
Journal Article
Journal Article