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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Autors principals: Solla, Paolo, Cannas, Antonino, Floris, Gianluca, Murru, Maria Rita, Corongiu, Daniela, Tranquilli, Stefania, Cuccu, Stefania, Rolesu, Marcella, Marrosu, Francesco, Marrosu, Maria Giovanna
Format: Artigo
Idioma:Inglês
Publicat: SAGE-Hindawi Access to Research 2010
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Research Article
Accés en línia: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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