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Lrrk2 modulation of Wnt signaling during zebrafish development
Mutations in leucine-rich repeat kinase 2 (lrrk2) are the most common genetic cause of Parkinson’s disease. Difficulty in elucidating the pathogenic mechanisms resulting from disease-associated Lrrk2 variants stems from the complexity of Lrrk2 function and activities. Lrrk2 contains multiple protein...
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| Publicado no: | J Neurosci Res |
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| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7643907/ https://ncbi.nlm.nih.gov/pubmed/32623786 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/jnr.24687 |
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