Sequencing of DISC1 pathway genes reveals increased burden of rare missense variants in schizophrenia patients from a northern Swedish population.

Sequencing of DISC1 pathway genes reveals increased burden of rare missense variants in schizophrenia patients from a northern Swedish population.

In recent years, DISC1 has emerged as one of the most credible and best supported candidate genes for schizophrenia and related neuropsychiatric disorders. Furthermore, increasing evidence--both genetic and functional--indicates that many of its protein interaction partners are also involved in the...

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Bibliographic Details
Main Authors: Lotte N Moens, Peter De Rijk, Joke Reumers, Maarten J A Van den Bossche, Wim Glassee, Sonia De Zutter, An-Sofie Lenaerts, Annelie Nordin, Lars-Göran Nilsson, Ignacio Medina Castello, Karl-Fredrik Norrback, Dirk Goossens, Kristel Van Steen, Rolf Adolfsson, Jurgen Del-Favero
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2011-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3154939?pdf=render

Internet

http://europepmc.org/articles/PMC3154939?pdf=render

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