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α - synuclein and Parkinson’s disease: the first roadblock

α-synuclein gene mutations are major underlying genetic defects known in familial juvenile onset Parkinson’s disease (PD), and α-synuclein is a major constituent of Lewy Bodies, the pathological hallmark of PD. The normal cellular function of α-synuclein has been elusive, and its exact etiological m...

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Bibliografiska uppgifter
Huvudupphovsmän: Lin Chua, Christelle En, Tang, Bor Luen
Materialtyp: Artigo
Språk:Inglês
Publicerad: John Wiley & Sons, Ltd 2006
Ämnen:
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC3933078/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2755/jcmm010.004.04
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