The Ala53Thr mutation in the α-synuclein gene in a Korean family with Parkinson disease
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.2007.00781.x/fullpdf
Reference12 articles.
1. Mutation in the alpha-synuclein gene identified in families with Parkinson’s disease;Polymeropoulos;Science,1997
2. Genetic analysis of families with Parkinson disease that carry the Ala53Thr mutation in the gene encoding alpha-synuclein;Athanassiadou;Am J Hum Genet,1999
3. Clinical features of parkinsonian patients with the alpha-synuclein (G209A) mutation;Bostantjopoulou;Mov Disord,2001
4. The new mutation, E46K, of alpha-synuclein causes Parkinson and Lewy body dementia;Zarranz;Ann Neurol,2004
5. Ala30Pro mutation in the gene encoding alpha-synuclein in Parkinson’s disease;Kruger;Nat Genet,1998
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