Analysis of Parkinson disease patients from Portugal for mutations in SNCA, PRKN, PINK1 and LRRK2

BACKGROUND: Mutations in the genes PRKN and LRRK2 are the most frequent known genetic lesions among Parkinson's disease patients. We have previously reported that in the Portuguese population the LRRK2 c.6055G > A; p.G2019S mutation has one of the highest frequencies in Europe. METHODS: Here...

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Detalles Bibliográficos
Autores principales: Bras, Jose, Guerreiro, Rita, Ribeiro, Maria, Morgadinho, Ana, Januario, Cristina, Dias, Margarida, Calado, Ana, Semedo, Cristina, Oliveira, Catarina, Hardy, John, Singleton, Andrew
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2248204/
https://www.ncbi.nlm.nih.gov/pubmed/18211709
http://dx.doi.org/10.1186/1471-2377-8-1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2248204/
https://www.ncbi.nlm.nih.gov/pubmed/18211709
http://dx.doi.org/10.1186/1471-2377-8-1

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