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LRRK2 function on actin and microtubule dynamics in Parkinson disease
The mutations in the LRRK2 gene cause clinically typical, late-onset Parkinson disease, strengthening the idea that the familial forms of the disease represent an important tool for the study of the idiopathic forms. Despite the great effort to describe and functionally characterize the LRRK2 gene p...
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| Hlavní autoři: | , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Landes Bioscience
2010
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2974064/ https://ncbi.nlm.nih.gov/pubmed/21057624 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4161/cib.3.5.12286 |
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