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
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Homann Carl
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Ott Erwin
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- Find related publications in this database (using NLM MeSH Indexing)
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DNA-Binding Proteins - genetics
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Dopamine - metabolism
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Exons - metabolism
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Family Health - metabolism
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Humans - metabolism
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Parkinson Disease - genetics
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Point Mutation - genetics
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Transcription Factors - genetics
- Find related publications in this database (Keywords)
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NR4A2 gene
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point mutations
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familial Parkinson's disease