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Neuropsychologia, ISSN 0028-3932, 01/2020, Volume 136, p. 107238
Huntington's Disease Like-2 (HDL2) is a rare autosomal dominant genetic disease caused by a mutation in the JPH3 gene. The Huntington's Disease (HD) phenocopy... 
Neuropsychology | Huntington's disease-like 2 | Huntington's disease | Single-case control design
Journal Article
Journal Article
Neuron, ISSN 0896-6273, 2011, Volume 70, Issue 3, pp. 427 - 440
Journal Article
Journal of Huntington's Disease, ISSN 1879-6397, 2017, Volume 6, Issue 1, pp. 37 - 46
Background: Huntington Disease-like 2 (HDL2) is a neurodegenerative disorder similar to Huntington Disease (HD) in its clinical phenotype, genetic... 
Acanthocytosis | chorea | HDL2 | Huntington's disease | Huntington disease-like 2 | junctophilin-3 | Literature reviews | Genotype & phenotype | Phenotypes | Basal ganglia | Neurodegenerative diseases | Chorea | Central nervous system diseases | Dementia disorders | Eye movements | Movement disorders
Journal Article
NEUROEPIDEMIOLOGY, ISSN 0251-5350, 2016, Volume 46, Issue 3, pp. 198 - 202
Background: Huntington disease (HD) has most recently been estimated to affect between 10.6 and 13.7 per 100,000 individuals in European populations. However,... 
Prevalence | REPEAT | Huntington disease-like 2 | Africa | Huntington disease | PHENOCOPIES | CLINICAL NEUROLOGY | PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH | HAPLOTYPE ANALYSIS | GENE | Frequency | South Africa | Occurrence | CAG-EXPANSION
Journal Article
Journal of Clinical Neuroscience, ISSN 0967-5868, 01/2018, Volume 47, pp. 126 - 127
Huntington's disease-like 2 (HDL2) is a rare autosomal dominant progressive neurodegenerative disorder commonly seen in adults. It was first described in a... 
HDL2 | HD | Huntington's disease | Huntington's disease-like 2 | Botswana | REPEAT EXPANSION | HUNTINGTON-DISEASE-LIKE-2 | NEUROSCIENCES | CLINICAL NEUROLOGY | Nervous system diseases | Genetic aspects | Genes | Liberalism
Journal Article
Movement Disorders, ISSN 0885-3185, 07/2007, Volume 22, Issue 10, pp. 1416 - 1423
Huntington's disease like‐2 (HDL‐2) neurodegeneration is a recently described autosomal dominant disorder with features similar to Huntington's disease (HD).... 
triple‐repeat | Huntington's disease‐like 2 | Huntington's disease | neuropathology | Triple-repeat | Huntington's disease-like 2 | Neuropathology | triple-repeat | CLINICAL NEUROLOGY | CHOREA-ACANTHOCYTOSIS | Humans | Huntington Disease - pathology | Brain - pathology | Huntington Disease - genetics | Trinucleotide Repeat Expansion - genetics | Adult | Family Health | Male
Journal Article
Journal of Clinical Neuroscience, ISSN 0967-5868, 01/2018, Volume 47, pp. 126 - 127
Huntington’s disease-like 2 (HDL2) is a rare autosomal dominant progressive neurodegenerative disorder commonly seen in adults. It was first described in a... 
Huntington’s disease-like 2 | Huntington’s disease | HDL2 | Botswana
Journal Article
Current Opinion in Neurology, ISSN 1350-7540, 11/2016, Volume 29, Issue 6, pp. 743 - 748
Purpose of review Huntington's disease-like 2 (HDL2) is a rare, progressive, autosomal dominant neurodegenerative disorder that genetically, clinically, and... 
Trinucleotide repeats | RNA toxicity | Bidirectional transcription | Protein toxicity | PROTEIN | HDL2 | RNA | REPEAT | HUNTINGTONS-DISEASE-LIKE-2 | trinucleotide repeats | NEUROSCIENCES | CLINICAL NEUROLOGY | JUNCTOPHILIN-3 | protein toxicity | GENE | HUNTINGTON-DISEASE-LIKE-2 | TRANSCRIPT | MUTATIONS | bidirectional transcription
Journal Article
Journal of Proteome Research, ISSN 1535-3893, 09/2016, Volume 15, Issue 9, pp. 3266 - 3283
The pathogenesis of HD and HDL2, similar progressive neurodegenerative disorders caused by expansion mutations, remains incompletely understood. No systematic... 
iTRAQ | human brain | Huntington’s disease | neurodegenerative disorder | TMT | proteomics
Journal Article