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An Early Axonopathy in a hLRRK2(R1441G) Transgenic Model of Parkinson Disease

Mutations in the gene for LRRK2 are the most common cause of familial Parkinson’s disease (PD) and patients with these mutations manifest clinical features that are indistinguishable from those of the more common sporadic form. Thus, investigations of disease mechanisms based on disease-causing LRRK...

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Dettagli Bibliografici
Pubblicato in:Neurobiol Dis
Autori principali: Tagliaferro, Patricia, Kareva, Tatyana, Oo, Tinmarla F, Yarygina, Olga, Kholodilov, Nikolai, Burke, Robert E
Natura: Artigo
Lingua:Inglês
Pubblicazione: 2015
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC4640977/
https://ncbi.nlm.nih.gov/pubmed/26192625
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.nbd.2015.07.009
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