A Genomic Pathway Approach to a Complex Disease: Axon Guidance and Parkinson Disease

While major inroads have been made in identifying the genetic causes of rare Mendelian disorders, little progress has been made in the discovery of common gene variations that predispose to complex diseases. The single gene variants that have been shown to associate reproducibly with complex disease...

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Detalhes bibliográficos
Main Authors: Lesnick, Timothy G, Papapetropoulos, Spiridon, Mash, Deborah C, Ffrench-Mullen, Jarlath, Shehadeh, Lina, de Andrade, Mariza, Henley, John R, Rocca, Walter A, Ahlskog, J. Eric, Maraganore, Demetrius M
Formato: Artigo
Idioma:Inglês
Publicado em: Public Library of Science 2007
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1904362/
https://ncbi.nlm.nih.gov/pubmed/17571925
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pgen.0030098
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