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LRRK2 directing ER-to-Golgi transport? (ER)yES!
Mutations in leucine-rich repeat kinase 2 (LRRK2) represent the most frequent genetic lesions associated with Parkinson’s disease (PD). LRRK2 function and the pathogenic mechanisms of LRRK2 genetic mutations remain poorly understood. Cho et al report in this issue of The EMBO Journal a new interacti...
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| Publicado en: | EMBO J |
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| Autor principal: | |
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
BlackWell Publishing Ltd
2014
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4253518/ https://ncbi.nlm.nih.gov/pubmed/25201881 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.15252/embj.201489832 |
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