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Article (Scientific journals)
Extended mutation analysis and association studies of Nurr1 (NR4A2) in Parkinson disease.
Hering, R.; Petrovic, S.; Mietz, E.-M. et al.
2004 • In Neurology, 62 (7), p. 1231-2
Peer Reviewed verified by ORBi
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https://hdl.handle.net/10993/17141
DOI
10.1212/01.WNL.0000118285.18383.90
PubMed
15079038
 

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Keywords :
Aged; Cohort Studies; DNA Mutational Analysis; DNA-Binding Proteins/genetics; Exons; Female; Gene Frequency; Genotype; Humans; Introns; Male; Middle Aged; Nuclear Receptor Subfamily 4, Group A, Member 2; Parkinson Disease/genetics; Polymorphism, Genetic; Psychotic Disorders/genetics; Transcription Factors/genetics
Research center :
- Luxembourg Centre for Systems Biomedicine (LCSB): Clinical & Experimental Neuroscience (Krüger Group)
Disciplines :
Genetics & genetic processes
Author, co-author :
Hering, R.
Petrovic, S.
Mietz, E.-M.
Holzmann, C.
Berg, D.
Bauer, P.
Woitalla, D.
Muller, T.
Berger, K.
KRÜGER, Rejko ;  University of Luxembourg > Faculty of Science, Technology and Communication (FSTC) > Life Science Research Unit
Riess, O.
Language :
English
Title :
Extended mutation analysis and association studies of Nurr1 (NR4A2) in Parkinson disease.
Publication date :
2004
Journal title :
Neurology
ISSN :
0028-3878
eISSN :
1526-632X
Publisher :
Lippincott Williams & Wilkins, United States - Maryland
Volume :
62
Issue :
7
Pages :
1231-2
Peer reviewed :
Peer Reviewed verified by ORBi
Available on ORBilu :
since 27 June 2014

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