Parkin Exon Rearrangements and Sequence Variants in LRRK2 Mutations Carriers: Analysis on a Possible Modifier Effect on LRRK2 Penetrance

Mutations in LRRK2 represent the most common causes of Parkinson's disease (PD) identified to date, but their penetrance is incomplete and probably due to the presence of other genetic or environmental factors required for development of the disease. We analyzed the presence of parkin sequence...

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Detalles Bibliográficos
Autores principales: Solla, Paolo, Cannas, Antonino, Floris, Gianluca, Murru, Maria Rita, Corongiu, Daniela, Tranquilli, Stefania, Cuccu, Stefania, Rolesu, Marcella, Marrosu, Francesco, Marrosu, Maria Giovanna
Formato: Texto
Lenguaje:English
Publicado: SAGE-Hindawi Access to Research 2010
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2957242/
https://www.ncbi.nlm.nih.gov/pubmed/20976090
http://dx.doi.org/10.4061/2010/537698

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2957242/
https://www.ncbi.nlm.nih.gov/pubmed/20976090
http://dx.doi.org/10.4061/2010/537698

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