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Parkin mutations in a patient with hemiparkinsonism-hemiatrophy: A clinical-genetic and PET study
P. P. Pramstaller
*
, G. Künig, K. Leenders, M. Kann, K. Hedrich, P. Vieregge, C. G. Goetz,
C. Klein
*
Corresponding author for this work
21
Citations (Scopus)
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Medicine & Life Sciences
Dystonia
100%
Missense Mutation
87%
Age of Onset
80%
Exons
70%
Ligands
60%
Mutation
47%