Associated Papers
Mutant Parkin impairs mitochondrial function and morphology in human fibroblasts.
Grünewald A et al.
Plos One, 2010
Parkin disease: a phenotypic study of a large case series.
Khan NL et al.
Brain : a Journal of Neurology, 2003
Role of parkin mutations in 111 community-based patients with early-onset parkinsonism.
Kann M et al.
Annals of Neurology, 2002
A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe. French Parkinson's Disease Genetics Study Group and the European Consortium on Genetic Susceptibility in Parkinson's Disease.
Abbas N et al.
Human Molecular Genetics, 1999
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