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^*

^*Korrespondierende/r Autor/-in für diese Arbeit

4 Zitate (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.

Originalsprache	Englisch
Zeitschrift	European Journal of Neurology
Jahrgang	10
Ausgabenummer	5
ISSN	1351-5101
DOIs	https://doi.org/10.1046/j.1468-1331.2003.00671.x
Publikationsstatus	Veröffentlicht - 01.09.2003

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10.1046/j.1468-1331.2003.00671.x

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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

AN - SCOPUS:0142119362

SN - 1351-5101

VL - 10

JO - European Journal of Neurology

JF - European Journal of Neurology

IS - 5

ER -

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

Abstract

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