The analysis of the human genome facilitates the study of the relationship between genotypes and phenotypes. Research on diseases such as Parkinsonīs Disease (PD), partly determined by mutations and polymorphisms in several genes, requires a large number of DNA samples in conjunction with highly standardised clinical information. To support further discovery of genetic components of PD, the Competence Network on Parkinsonīs Disease (CNP e.V.) initiated the Gene Bank Parkinsonīs Disease Germany (GEPARD) and underwent a complex procedure to establish an internet-based data system that fulfils the legal requirements of the German data safety and protection laws.
Print ISSN: 1611-2776
Volume: 49, 06/2007
Pages: 367 - 373