NR4A2 mutations are rare among European patients with familial Parkinson's disease [1]

Claudia Wellenbrock; Katja Hedrich; Nora Schäfer; Meike Kasten; Helfried Jacobs; Eberhard Schwinger; Johann Hagenah; Peter P. Pramstaller; Peter Vieregge; Christine Klein

NR4A2 mutations are rare among European patients with familial Parkinson's disease [1]

Claudia Wellenbrock^*, Katja Hedrich, Nora Schäfer, Meike Kasten, Helfried Jacobs, Eberhard Schwinger, Johann Hagenah, Peter P. Pramstaller, Peter Vieregge, Christine Klein

^*Corresponding author for this work

26 Citations (Scopus)

Original language	English
Journal	Annals of Neurology
Volume	54
Issue number	3
ISSN	0364-5134
Publication status	Published - 01.09.2003

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

SDG 3 Good Health and Well-being
SDG 10 Reduced Inequalities

Cite this

@article{07893ed463d4481c919a197997644e27,

title = "NR4A2 mutations are rare among European patients with familial Parkinson's disease [1]",

author = "Claudia Wellenbrock and Katja Hedrich and Nora Sch{\"a}fer and Meike Kasten and Helfried Jacobs and Eberhard Schwinger and Johann Hagenah and Pramstaller, \{Peter P.\} and Peter Vieregge and Christine Klein",

year = "2003",

month = sep,

day = "1",

language = "English",

volume = "54",

journal = "Annals of Neurology",

issn = "0364-5134",

publisher = "John Wiley \& Sons Inc.",

number = "3",

}

TY - JOUR

T1 - NR4A2 mutations are rare among European patients with familial Parkinson's disease [1]

AU - Wellenbrock, Claudia

AU - Hedrich, Katja

AU - Schäfer, Nora

AU - Kasten, Meike

AU - Jacobs, Helfried

AU - Schwinger, Eberhard

AU - Hagenah, Johann

AU - Pramstaller, Peter P.

AU - Vieregge, Peter

AU - Klein, Christine

PY - 2003/9/1

Y1 - 2003/9/1

UR - https://www.scopus.com/pages/publications/0042336994

M3 - Letters

C2 - 12953278

AN - SCOPUS:0042336994

SN - 0364-5134

VL - 54

JO - Annals of Neurology

JF - Annals of Neurology

IS - 3

ER -

NR4A2 mutations are rare among European patients with familial Parkinson's disease [1]

UN SDGs

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