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Differential effects of PINK1 nonsense and missense mutations on mitochondrial function and morphology
A. Grünewald, M. E. Gegg, J. W. Taanman, R. H. King, N. Kock,
C. Klein
, A. H.V. Schapira
*
*
Corresponding author for this work
Clinic of Neurology
Institute of Neurogenetics
Institute of Neurology
University of London
77
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Biochemistry, Genetics and Molecular Biology
Morphology
100%
Nonsense Mutation
100%
Missense Mutation
100%
PINK1
100%
Mutant
40%
Wild Type
20%
Enzyme
20%
Gene
20%
Phosphotransferase
20%
Autosomal Recessive Inheritance
20%
Missense
20%
Fibroblast Culture
20%
Neuroscience
Metabolic Pathway
100%
Gene
100%
Mitochondrial Function
100%
Fibroblast
100%
Parkinson's Disease
100%