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LRRK2 Pathobiology in Parkinson’s Disease

Mutations in the catalytic Roc-COR and kinase domains of leucine-rich repeat kinase 2 (LRRK2) are a common cause of familial Parkinson’s disease (PD). LRRK2 mutations cause PD with age-related penetrance and clinical features identical to late-onset sporadic PD. Biochemical studies support an increa...

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Bibliografski detalji
Izdano u:J Neurochem
Glavni autori: Martin, Ian, Kim, Jungwoo Wren, Dawson, Valina L., Dawson, Ted M.
Format: Artigo
Jezik:Inglês
Izdano: 2014
Teme:
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC4237709/
https://ncbi.nlm.nih.gov/pubmed/25251388
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/jnc.12949
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