Clinical features of Chinese patients with Huntington's disease carrying CAG repeats beyond 60 within HTT gene

scientific article published on 11 March 2013

Clinical features of Chinese patients with Huntington's disease carrying CAG repeats beyond 60 within HTT gene is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1111/CGE.12120
P698PubMed publication ID23398026

P2093author name stringZ-J Liu
Y Dong
Z-Y Wu
Y-M Sun
W Ni
S-S Shi
P2860cites workA novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes.Q27860836
Psychiatric and cognitive difficulties as indicators of juvenile huntington disease onset in 29 patientsQ31115405
Biological and clinical manifestations of Huntington's disease in the longitudinal TRACK-HD study: cross-sectional analysis of baseline dataQ33489152
High frequency of Machado-Joseph disease identified in southeastern Chinese kindreds with spinocerebellar ataxiaQ33545469
Juvenile onset Huntington's disease--clinical and research perspectives.Q34091006
Trinucleotide repeat length instability and age of onset in Huntington's diseaseQ34357407
The Prevalence of Juvenile Huntington's Disease: A Review of the Literature and Meta-Analysis.Q34406943
Juvenile Huntington's disease: does a dosage-effect pathogenic mechanism differ from the classical adult disease?Q36308082
Seizures in juvenile Huntington's disease: frequency and characterization in a multicenter cohortQ38057665
The gender effect in juvenile Huntington disease patients of Italian originQ44750677
MR imaging and spectroscopy in juvenile Huntington diseaseQ44813179
Juvenile Huntington disease exacerbated by methylphenidate: case report.Q45290270
Excessive blinking as an initial manifestation of juvenile Huntington's diseaseQ45290961
Genetic testing of children at risk for Huntington's disease. US Huntington Disease Genetic Testing GroupQ45295162
Intergeneration CAG expansion and contraction in a Chinese HD family.Q45300267
Clinical presentation of juvenile Huntington diseaseQ45300768
Atypical movement disorders in the early stages of Huntington's disease: clinical and genetic analysisQ45301042
Huntington disease in children: genotype-phenotype correlationQ45301605
Speech and language delay are early manifestations of juvenile-onset Huntington diseaseQ45302788
The relationship between CAG repeat length and age of onset differs for Huntington's disease patients with juvenile onset or adult onset.Q45303652
Age, CAG repeat length, and clinical progression in Huntington's diseaseQ45305597
Juvenile Huntington disease in an 18-month-old boy revealed by global developmental delay and reduced cerebellar volumeQ57083854
Unified Huntington's disease rating scale: Reliability and consistencyQ57422462
P433issue2
P921main subjectHuntington's diseaseQ190564
P304page(s)189-193
P577publication date2013-03-11
P1433published inClinical GeneticsQ5133760
P1476titleClinical features of Chinese patients with Huntington's disease carrying CAG repeats beyond 60 within HTT gene
P478volume85

Reverse relations

cites work (P2860)
Q45305006A survey-based study identifies common but unrecognized symptoms in a large series of juvenile Huntington's disease
Q90599532Clinical and Genetic Profiles in Chinese Patients with Huntington's Disease: A Ten-year Multicenter Study in China
Q39061929Development of Research on Huntington Disease in China
Q45297225Huntingtin gene CAG repeat numbers in Chinese patients with Huntington's disease and controls
Q36523129Huntington Disease in Asia
Q38689609Huntington's Disease: Relationship Between Phenotype and Genotype
Q41317971Tics as an initial manifestation of juvenile Huntington's disease: case report and literature review

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