The search for modifier genes in Huntington disease – Multifactorial aspects of a monogenic disorder
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology
Reference67 articles.
1. Identifying modifier genes of monogenic disease: strategies and difficulties;Génin;Hum. Genet.,2008
2. A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes;Cell,1993
3. Reduced penetrance of the Huntington's disease mutation;McNeil;Hum. Mol. Genet.,1997
4. Trinucleotide repeat length instability and age of onset in Huntington's disease;Duyao;Nat. Genet.,1993
5. Huntington's disease;Gusella;Semin. Cell Biol.,1995
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