Heterozygous mutations in genes causing parkinsonism: monogenic disorders go complex
Author:
Publisher
Elsevier BV
Subject
Clinical Neurology
Reference5 articles.
1. The genetics of Parkinson disease;Klein;Nat Clin Pract Neurol,2006
2. Evaluation of LRRK2 G2019S penetrance: relevance for genetic counseling in Parkinson disease;Goldwurm;Neurology,2007
3. Deciphering the role of heterozygous mutations in genes associated with parkinsonism;Klein;Lancet Neurol,2007
4. Beyond Mendel: an evolving view of human genetic disease transmission;Badano;Nat Rev Genet,2002
5. LRRK2 G2019S as a cause of Parkinson's disease in North African Arabs;Lesage;N Engl J Med,2006
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