G2019S LRRK2 mutation causing Parkinson's disease without Lewy bodies

The G2019S leucine‐rich repeat kinase 2 gene (LRRK2) mutation has been identified in a significant proportion of familial and sporadic cases of Parkinson's disease (PD). Until now, information on the neuropathological changes associated with the G2019S LRRK2 mutation has been sparse. We report...

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Kaydedildi:
Detaylı Bibliyografya
Asıl Yazarlar: Gaig, Carles, Martí, María José, Ezquerra, Mario, Rey, Maria Jesús, Cardozo, Adriana, Tolosa, Eduardo
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: BMJ Group 2007
Konular:
Short Report
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC2077973/
https://ncbi.nlm.nih.gov/pubmed/17210620
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jnnp.2006.107904
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