Abstract
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 language | English |
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Journal | European Journal of Neurology |
Volume | 10 |
Issue number | 5 |
ISSN | 1351-5101 |
DOIs | |
Publication status | Published - 01.09.2003 |