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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Publicat a:Sci Rep
Autors principals: 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.
Format: Artigo
Idioma:Inglês
Publicat: Nature Publishing Group UK 2018
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Article
Accés en línia: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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