Point mutations in exon 1 of the NR4A2 gene are not a major cause of familial Parkinson's disease
| Autor: | Nikolaus Homann, Thomas Gasser, Claudia Trenkwalder, Gyri Wieditz, Alexander Zimprich, Erwin Ott, A. Wijnand F. Rutgers, Mirna Castro, Friedrich Asmus, Petra Leitner, Benjamin Bereznai |
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| Rok vydání: | 2003 |
| Předmět: |
Genetics
Family Health Parkinson's disease business.industry Point mutation Dopamine Parkinson Disease Exons medicine.disease Nr4a2 gene Molecular medicine Human genetics DNA-Binding Proteins Cellular and Molecular Neuroscience Exon Nuclear Receptor Subfamily 4 Group A Member 2 Medicine Humans Point Mutation business Genetics (clinical) Transcription Factors |
| Zdroj: | Neurogenetics. 4(4) |
| ISSN: | 1364-6745 |
| Databáze: | OpenAIRE |
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