American Journal of Medical Genetics Part B Neuropsychiatric Genetics · 2006 · 11 citations · 9 references
Life SciencesGeneticsMolecular GeneticsHuman GeneticsMedical GeneticsNeurogeneticsGenetic DisordersGenetic SyndromesHuntington DiseaseMendelian DisordersNeurodegenerative DiseasesNeurogenetic DisordersFamilial Neurodegenerative DiseaseGermline MutationsGermline PredispositionJuvenile Huntington DiseaseMaternal Transmission BiasPaternal TransmissionRepeat Expansion DisordersRepeat Expansion Mutations
The prevalence of juvenile-onset Huntington's disease (HD) is about ten times lower than adult HD. Here we report a Chinese HD family showing both intergeneration CAG expansion and contraction. The expansion resulted from a paternal transmission which leads to juvenile-onset HD for a 17-year-old Chinese boy (III-5). More interestingly, a contraction was noticed in a maternal transmission (III-3), which changed the CAG repeat from an expanded, disease-causing allele (48 repeats) to a normal or intermediate allele (34 repeats). Of note, the contraction resulted in a deletion of 14 CAG repeats, which is much larger than previously reported contractions. Our results are consistent with previous observations in Western Caucasians that juvenile-onset HD is more likely inherited through the male germline.
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David C. Rubinsztein, Jayne Leggo, Rhian Coles et al. · HAL (Le Centre pour la Communication Scientifique Directe) · 1996 · 468 citations
A functional variant of SUMO4, a new IκBα modifier, is associated with type 1 diabetes
Dehuang Guo, Manyu Li, Yan Zhang et al. · Nature Genetics · 2004 · 422 citations