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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
Institute of Neurogenetics
European Academy Bozen
Zurich Center for Integrative Human Physiology (ZIHP)
University of Groningen
Department of Neurological Science
Rush Medical College
32
Citations (Scopus)
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Medicine and Dentistry
Polyethylene Terephthalate
100%
Parkin
100%
Parkinsonism
100%
Radioactive Tracer
33%
Exon
33%
Receptor
33%
Dystonia
33%
Onset Age
33%
Genetic Analysis
33%
Missense Mutation
33%