Balance is the challenge - The impact of mitochondrial dynamics in Parkinson’s disease
Author:
Publisher
Wiley
Subject
Clinical Biochemistry,Biochemistry,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2362.2010.02354.x/fullpdf
Reference109 articles.
1. Review: Familial Parkinson’s disease--genetics, clinical phenotype and neuropathology in relation to the common sporadic form of the disease;Schiesling;Neuropathol Appl Neurobiol,2008
2. Genome-wide association study reveals genetic risk underlying Parkinson’s disease;Simon-Sanchez;Nat Genet,2009
3. Mitochondria in the aetiology and pathogenesis of Parkinson’s disease;Schapira;Parkinsonism Relat Disord,1999
4. Loss of function mutations in the gene encoding Omi/HtrA2 in Parkinson’s disease;Strauss;Hum Mol Genet,2005
5. PINK1 mutations are associated with sporadic early-onset parkinsonism;Valente;Ann Neurol,2004
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