Common genetic variation in Neuregulin 3 (NRG3) influences risk for schizophrenia and impacts NRG3 expression in human brain

Structural and polymorphic variations in Neuregulin 3 (NRG3), 10q22-23 are associated with a broad spectrum of neurodevelopmental disorders including developmental delay, cognitive impairment, autism, and schizophrenia. NRG3 is a member of the neuregulin family of EGF proteins and a ligand for the E...

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Hlavní autoři: Kao, Wee-Tin, Wang, Yanhong, Kleinman, Joel E., Lipska, Barbara K., Hyde, Thomas M., Weinberger, Daniel R., Law, Amanda J.
Médium: Artigo
Jazyk:Inglês
Vydáno: National Academy of Sciences 2010
Témata:
Biological Sciences
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC2932571/
https://ncbi.nlm.nih.gov/pubmed/20713722
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.1005410107
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