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In silico comparative analysis of LRRK2 interactomes from brain, kidney and lung
Mutations in LRRK2 are the most frequent cause of familial Parkinson’s disease (PD), with common LRRK2 non-coding variants also acting as risk factors for idiopathic PD. Currently, therapeutic agents targeting LRRK2 are undergoing advanced clinical trials in humans, however, it is important to under...
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| Publicado no: | Brain Res |
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| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Elsevier/North-Holland Biomedical Press
2021
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8212912/ https://ncbi.nlm.nih.gov/pubmed/33915162 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.brainres.2021.147503 |
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