A systematic screening to identify de novo mutations causing sporadic early-onset Parkinson's disease

Despite the many advances in our understanding of the genetic basis of Mendelian forms of Parkinson's disease (PD), a large number of early-onset cases still remain to be explained. Many of these cases, present with a form of disease that is identical to that underlined by genetic causes, but d...

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Detalles Bibliográficos
Autores principales: Kun-Rodrigues, Celia, Ganos, Christos, Guerreiro, Rita, Schneider, Susanne A., Schulte, Claudia, Lesage, Suzanne, Darwent, Lee, Holmans, Peter, Singleton, Andrew, Bhatia, Kailash, Bras, Jose
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2015
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4634375/
https://www.ncbi.nlm.nih.gov/pubmed/26362251
http://dx.doi.org/10.1093/hmg/ddv376

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4634375/
https://www.ncbi.nlm.nih.gov/pubmed/26362251
http://dx.doi.org/10.1093/hmg/ddv376

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