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Transgenic LRRK2(R1441G) rats–a model for Parkinson disease?
Parkinson disease (PD) is the most common movement disorder, characterized by the progressive degeneration of dopaminergic neurons in the substantia nigra. While the cause of this disease is largely unknown, a rare autosomal dominant familial form of PD is caused by a genetic mutation in the leucine...
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| Publicado no: | PeerJ |
|---|---|
| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
PeerJ Inc.
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4435452/ https://ncbi.nlm.nih.gov/pubmed/26020005 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7717/peerj.945 |
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