Loss of Nuclear Activity of the FBXO7 Protein in Patients with Parkinsonian-Pyramidal Syndrome (PARK15)

Mutations in the F-box only protein 7 gene (FBXO7) cause PARK15, an autosomal recessive neurodegenerative disease presenting with severe levodopa-responsive parkinsonism and pyramidal disturbances. Understanding the PARK15 pathogenesis might thus provide clues on the mechanisms of maintenance of bra...

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Detalles Bibliográficos
Autores principales: Zhao, Tianna, De Graaff, Esther, Breedveld, Guido J., Loda, Agnese, Severijnen, Lies-Anne, Wouters, Cokkie H., Verheijen, Frans W., Dekker, Marieke C. J., Montagna, Pasquale, Willemsen, Rob, Oostra, Ben A., Bonifati, Vincenzo
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3037939/
https://www.ncbi.nlm.nih.gov/pubmed/21347293
http://dx.doi.org/10.1371/journal.pone.0016983

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3037939/
https://www.ncbi.nlm.nih.gov/pubmed/21347293
http://dx.doi.org/10.1371/journal.pone.0016983

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