Exclusion of PINK1 as candidate gene for the late-onset form of Parkinson's disease in two European populations

BACKGROUND: Parkinson's disease (PD) is the second most common neurodegenerative disorder. Recently, mutations in the PINK1 (PARK6) gene were shown to rarely cause autosomal-recessively transmitted, early-onset parkinsonism. In order to evaluate whether PINK1 contributes to the risk of common l...

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Detalles Bibliográficos
Autores principales: Schlitter, Anna Melissa, Kurz, Martin, Larsen, Jan P, Woitalla, Dirk, Mueller, Thomas, Epplen, Joerg T, Dekomien, Gabriele
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2005
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1325256/
https://www.ncbi.nlm.nih.gov/pubmed/16354302
http://dx.doi.org/10.1186/1477-5751-4-10

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1325256/
https://www.ncbi.nlm.nih.gov/pubmed/16354302
http://dx.doi.org/10.1186/1477-5751-4-10

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