Huntington disease in subjects from an Israeli Karaite community carrying alleles of intermediate and expanded CAG repeats in the HTT gene: Huntington disease or phenocopy?
Author:
Publisher
Elsevier BV
Subject
Clinical Neurology,Neurology
Reference21 articles.
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3. Homozygosity for CAG mutation in Huntington disease is associated with a more severe clinical course;Squitieri;Brain,2003
4. Expansion of a 27 CAG repeat allele into a symptomatic Huntington disease-producing allele;Kelly;Am J Med Genet,1999
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