| P50 | author | Jan Roth | Q45291752 |
| | Jan Stochl | Q42306065 |
| P2093 | author name string | Jiří Klempíř | |
| | Jana Zidovská | |
| | Tereza Uhrová | |
| | Věra Kebrdlová Ing | |
| P2860 | cites work | Somatic and gonadal mosaicism of the Huntington disease gene CAG repeat in brain and sperm. | Q42496337 |
| | Dramatic tissue-specific mutation length increases are an early molecular event in Huntington disease pathogenesis | Q44626605 |
| | Hand tapping: a simple, reproducible, objective marker of motor dysfunction in Huntington's disease. | Q45289512 |
| | A new polymerase chain reaction (PCR) assay for the trinucleotide repeat that is unstable and expanded on Huntington's disease chromosomes | Q45290738 |
| | Relationship between trinucleotide repeat expansion and phenotypic variation in Huntington's disease | Q45290871 |
| | Trinucleotide repeat length and clinical progression in Huntington's disease | Q45291777 |
| | A new model for prediction of the age of onset and penetrance for Huntington's disease based on CAG length. | Q45292888 |
| | A European pilot quality assessment scheme for molecular diagnosis of Huntington's disease | Q45298054 |
| | The expanded CAG repeat associated with juvenile Huntington disease shows a common origin of most or all neurons and glia in human cerebrum. | Q45300454 |
| | Age-dependent and tissue-specific CAG repeat instability occurs in mouse knock-in for a mutant Huntington's disease gene | Q45303594 |
| | The relationship between CAG repeat length and age of onset differs for Huntington's disease patients with juvenile onset or adult onset. | Q45303652 |
| | Bradykinesia in Huntington's disease. A prospective, follow-up study | Q45305825 |
| | Cognitive changes in asymptomatic carriers of the Huntington disease mutation gene | Q45306713 |
| | CAG expansion affects the expression of mutant Huntingtin in the Huntington's disease brain | Q45307352 |
| | Interaction of normal and expanded CAG repeat sizes influences age at onset of Huntington disease | Q57628958 |
| | Huntingtin-associated protein-1 is a modifier of the age-at-onset of Huntington's disease | Q24306416 |
| | A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes. | Q27860836 |
| | The relationship between trinucleotide (CAG) repeat length and clinical features of Huntington's disease | Q28264134 |
| | Normal huntingtin function: an alternative approach to Huntington's disease | Q28281904 |
| | Evidence for a modifier of onset age in Huntington disease linked to the HD gene in 4p16. | Q30445013 |
| | Genome-wide significance for a modifier of age at neurological onset in Huntington's disease at 6q23-24: the HD MAPS study | Q30445842 |
| | A genome scan for modifiers of age at onset in Huntington disease: The HD MAPS study. | Q30448206 |
| | Change in MRI striatal volumes as a biomarker in preclinical Huntington's disease | Q31105242 |
| | DNA instability in replicating Huntington's disease lymphoblasts | Q33408394 |
| | Molecular analysis of late onset Huntington's disease | Q33596065 |
| | Homozygosity for CAG mutation in Huntington disease is associated with a more severe clinical course | Q34181024 |
| | A polymorphic DNA marker genetically linked to Huntington's disease | Q34255139 |
| | Trinucleotide repeat length instability and age of onset in Huntington's disease | Q34357407 |
| | CAG-repeat length and the age of onset in Huntington disease (HD): a review and validation study of statistical approaches | Q34624785 |
| | Normal and mutant HTT interact to affect clinical severity and progression in Huntington disease | Q35004805 |
| | Psychiatric disorders in preclinical Huntington's disease | Q36227490 |
| | DNA instability in postmitotic neurons | Q36491349 |
| | Motor disorder in Huntington's disease begins as a dysfunction in error feedback control. | Q36914999 |
| | Mechanisms of neurodegeneration in Huntington's disease. | Q37202865 |
| | New Huntington disease mutation arising from a paternal CAG34 allele showing somatic length variation in serially passaged lymphoblasts | Q40491540 |
| P433 | issue | 1 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | Huntington's disease | Q190564 |
| P304 | page(s) | 125-129 | |
| P577 | publication date | 2010-11-10 | |
| P1433 | published in | Movement Disorders | Q1486418 |
| P1476 | title | The number of CAG repeats within the normal allele does not influence the age of onset in Huntington's disease | |
| P478 | volume | 26 | |