GIGYF2 mutation in late-onset Parkinson’s disease with cognitive impairment

Although in the last two decades there has been considerable progress in understanding the genetic basis of Parkinson’s disease (PD), the majority of PD is sporadic and its genetic causes are largely unknown. In an attempt to identify novel genetic causes of PD, whole exome sequencing and subsequent...

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Detalles Bibliográficos
Autores principales: Ruiz-Martinez, Javier, Krebs, Catharine E., Makarov, Vladimir, Gorostidi, Ana, Martí-Massó, Jose Félix, Paisán-Ruiz, Coro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2015
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4624020/
https://www.ncbi.nlm.nih.gov/pubmed/26134514
http://dx.doi.org/10.1038/jhg.2015.69

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4624020/
https://www.ncbi.nlm.nih.gov/pubmed/26134514
http://dx.doi.org/10.1038/jhg.2015.69

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