Extended mutation analysis and association studies of Nurr1 (NR4A2) in Parkinson disease

Neurology. 2004 Apr 13;62(7):1231-2. doi: 10.1212/01.wnl.0000118285.18383.90.

Authors

R Hering¹, S Petrovic, E-M Mietz, C Holzmann, D Berg, P Bauer, D Woitalla, T Müller, K Berger, R Krüger, O Riess

Affiliation

¹ Department of Medical Genetics, Hertie Institute of Clinical Brain Research, University of Tübingen, Germany.

PMID: 15079038
DOI: 10.1212/01.wnl.0000118285.18383.90

No abstract available

Publication types

Research Support, Non-U.S. Gov't

MeSH terms

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*

Substances

DNA-Binding Proteins
NR4A2 protein, human
Nuclear Receptor Subfamily 4, Group A, Member 2
Transcription Factors