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

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

<p>Abstract</p> <p>Background</p> <p>Mutations in the genes <it>PRKN </it>and <it>LRRK2 </it>are the most frequent known genetic lesions among Parkinson's disease patients. We have previously reported that in the Portuguese population the &l...

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Bibliographic Details
Main Authors: Calado Ana, Dias Margarida, Januario Cristina, Morgadinho Ana, Ribeiro Maria, Guerreiro Rita, Bras Jose, Semedo Cristina, Oliveira Catarina, Hardy John, Singleton Andrew
Format: Article
Language:English
Published: BMC 2008-01-01
Series:BMC Neurology
Online Access:http://www.biomedcentral.com/1471-2377/8/1

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http://www.biomedcentral.com/1471-2377/8/1

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