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Jennifer a Collins

Frequency of the loss of CAA interruption in the HTT CAG tract and implications for Huntington disease in the reduced penetrance range
Interrupting sequence variants and age of onset in Huntington's disease: clinical implications and emerging therapies
Length of uninterrupted CAG, independent of polyglutamine size, results in increased somatic instability, hastening onset of Huntington disease
The molecular epidemiology of Huntington disease is related to intermediate allele frequency and haplotype in the general population
The targetable A1 Huntington disease haplotype has distinct Amerindian and European origins in Latin America

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