Regionally specific TSC1 and TSC2 gene expression in tuberous sclerosis complex

Tuberous sclerosis complex (TSC), a heritable neurodevelopmental disorder, is caused by mutations in the TSC1 or TSC2 genes. To date, there has been little work to elucidate regional TSC1 and TSC2 gene expression within the human brain, how it changes with age, and how it may influence disease. Usin...

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Publicado no:Sci Rep
Main Authors: Li, Yi, Barkovich, Matthew J., Karch, Celeste M., Nillo, Ryan M., Fan, Chun-Chieh, Broce, Iris J., Tan, Chin Hong, Cuneo, Daniel, Hess, Christopher P., Dillon, William P., Glenn, Orit A., Glastonbury, Christine M., Olney, Nicholas, Yokoyama, Jennifer S., Bonham, Luke W., Miller, Bruce, Kao, Aimee, Schmansky, Nicholas, Fischl, Bruce, Andreassen, Ole A., Jernigan, Terry, Dale, Anders, Barkovich, A. James, Desikan, Rahul S., Sugrue, Leo P.
Formato: Artigo
Idioma:Inglês
Publicado em: Nature Publishing Group UK 2018
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6127129/
https://ncbi.nlm.nih.gov/pubmed/30190613
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41598-018-31075-4
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