Unstable familial transmissions of Huntington disease alleles with 27-35 CAG repeats (intermediate alleles)
Author:
Publisher
Wiley
Subject
Cellular and Molecular Neuroscience,Psychiatry and Mental health,Genetics (clinical)
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.b.30970/fullpdf
Reference34 articles.
1. Ancestral differences in the distribution of the Δ2642 glutamic acid polymorphism is associated with varying CAG repeat lengths on normal chromosomes: Insights into the genetic evolution of Huntington disease;Almqvist;Hum Mol Genet,1995
2. High incidence rate and absent family histories in one quarter of patients newly diagnosed with Huntington disease in British Columbia;Almqvist;Clin Genet,2001
3. Origins and evolution of Huntington disease chromosomes;Andrew;Neurodegeneration,1995
4. Significant nonrandom allelic association between Huntington disease and two loci separated by at least 3 Mb on 4p16.3;Andrew;Genomics,1992
5. A CCG repeat polymorphism adjacent to the CAG repeat in the Huntington disease gene: Implications for diagnostic accuracy and predictive testing;Andrew;Hum Mol Genet,1994
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