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Parkinson’s Disease
Volume 2011, Article ID 827693, 6 pages
Research Article

Analysis of Nucleotide Variations in Genes of Iron Management in Patients of Parkinson's Disease and Other Movement Disorders

1Genomic Unit for the Diagnosis of Human Pathologies, Center for Genomics, Bioinformatics and Biostatistics, San Raffaele Scientific Institute, 20132 Milan, Italy
2Sezione di Chimica, Facoltà di Medicina, Università di Brescia & Terzo Laboratorio di Analisi Chimico Cliniche, Spedali Civili di Brescia, 25123 Brescia, Italy
3Centro Parkinson e Disturbi del Movimento, Istituti Clinici di Perfezionamento, 20126 Milan, Italy
4Centro della Microcitemia e Anemie Congenite, Ospedale Galliera, 16128 Genova, Italy
5Department of Clinical and Experimental Medicine, Section of Internal Medicine, University of Verona, 37134 Verona, Italy
6Università Vita-Salute San Raffaele, 20132 Milan, Italy
7Diagnostica e Ricerca San Raffaele SpA, Milan, Italy

Received 17 June 2010; Accepted 27 September 2010

Academic Editor: Carlo Colosimo

Copyright © 2011 Emanuela Castiglioni et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Supplementary Material

The supplementary data provide the sequence of all the primers used for PCR amplification of exons and intronic boundary regions of the different genes analysed in the study and the temperatures applied in the dHPLC analysis of each DNA fragment.

  1. Supplementary Table