SCA2 and SCA3 mutations in young-onset dopa-responsive parkinsonism

M. Svetel, A. Djarmati, N. Dragašević, D. Savić, B. Čuljković, S. Romac, V. S. Kostić*

*Corresponding author for this work
4 Citations (Scopus)


In this study no one of our 85 patients of Serbian origin with young-onset (≤ 45 years) dopa-responsive parkinsonism (YOP), previously proved negative for PARK1 and PARK2 mutations, had either spinocerebellar ataxia type 2 (SCA2) or SCA3 mutation. These data do not prove the significance of these two mutations in either sporadic or familial YOP suggestive of Parkinson's disease.

Original languageEnglish
JournalEuropean Journal of Neurology
Issue number5
Publication statusPublished - 01.09.2003


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