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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Hlavní autoři: 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
Médium: Artigo
Jazyk:Inglês
Vydáno: Public Library of Science 2007
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Research Article
On-line přístup: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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