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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Detalles Bibliográficos
Autores principales: 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: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6127129/
https://www.ncbi.nlm.nih.gov/pubmed/30190613
http://dx.doi.org/10.1038/s41598-018-31075-4

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6127129/
https://www.ncbi.nlm.nih.gov/pubmed/30190613
http://dx.doi.org/10.1038/s41598-018-31075-4

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