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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Detalhes bibliográficos
Main Authors: Solla, Paolo, Cannas, Antonino, Floris, Gianluca, Murru, Maria Rita, Corongiu, Daniela, Tranquilli, Stefania, Cuccu, Stefania, Rolesu, Marcella, Marrosu, Francesco, Marrosu, Maria Giovanna
Formato: Artigo
Idioma:Inglês
Publicado em: SAGE-Hindawi Access to Research 2010
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2957242/
https://ncbi.nlm.nih.gov/pubmed/20976090
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4061/2010/537698
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