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Gewählte Publikation:

Zimprich, A; Asmus, F; Leitner, P; Castro, M; Bereznai, B; Homann, N; Ott, E; Rutgers, AW; Wieditz, G; Trenkwalder, C; Gasser, T.
Point mutations in exon 1 of the NR4A2 gene are not a major cause of familial Parkinson's disease.
Neurogenetics. 2003; 4(4):219-220 Doi: 10.1007/s10048-003-0156-x
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Co-Autor*innen der Med Uni Graz
Homann Carl
Ott Erwin
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Find related publications in this database (using NLM MeSH Indexing)
DNA-Binding Proteins - genetics
Dopamine - metabolism
Exons - metabolism
Family Health - metabolism
Humans - metabolism
Parkinson Disease - genetics
Point Mutation - genetics
Transcription Factors - genetics

Find related publications in this database (Keywords)
NR4A2 gene
point mutations
familial Parkinson's disease
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