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

doi:10.1046/j.1468-1331.2003.00671.x

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

Institute of Neurogenetics

4 Citations (Scopus)

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
Journal	European Journal of Neurology
Volume	10
Issue number	5
ISSN	1351-5101
DOIs	https://doi.org/10.1046/j.1468-1331.2003.00671.x
Publication status	Published - 01.09.2003

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title = "SCA2 and SCA3 mutations in young-onset dopa-responsive parkinsonism",

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.",

author = "M. Svetel and A. Djarmati and N. Draga{\v s}evi{\'c} and D. Savi{\'c} and B. {\v C}uljkovi{\'c} and S. Romac and Kosti{\'c}, {V. S.}",

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AU - Svetel, M.

AU - Djarmati, A.

AU - Dragašević, N.

AU - Savić, D.

AU - Čuljković, B.

AU - Romac, S.

AU - Kostić, V. S.

PY - 2003/9/1

Y1 - 2003/9/1

N2 - 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.

AB - 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.

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U2 - 10.1046/j.1468-1331.2003.00671.x

DO - 10.1046/j.1468-1331.2003.00671.x

M3 - Journal articles

C2 - 12940846

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VL - 10

JO - European Journal of Neurology

JF - European Journal of Neurology

SN - 1351-5101

IS - 5

ER -

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

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