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The role of monogenic genes in idiopathic Parkinson’s disease

In the past two decades, mutations in multiple genes have been linked to autosomal dominant or recessive forms of monogenic Parkinson’s disease (PD). Collectively, these monogenic (often familial) cases account for less than 5% of all PD, the majority being apparently sporadic cases. More recently,...

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Kaydedildi:
Detaylı Bibliyografya
Yayımlandı:Neurobiol Dis
Asıl Yazarlar: Reed, Xylena, Bandrés-Ciga, Sara, Blauwendraat, Cornelis, Cookson, Mark R.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 2018
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC6363864/
https://ncbi.nlm.nih.gov/pubmed/30448284
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.nbd.2018.11.012
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