Complex Neurological Phenotype in Mutant Mice Lacking Tsc2 in Excitatory Neurons of the Developing Forebrain(123)

Mutations in the TSC1 and TSC2 genes cause tuberous sclerosis complex (TSC), a genetic disease often associated with epilepsy, intellectual disability, and autism, and characterized by the presence of anatomical malformations in the brain as well as tumors in other organs. The TSC1 and TSC2 proteins...

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Detalles Bibliográficos
Autores principales: Crowell, Beth, Hwa Lee, Gum, Nikolaeva, Ina, Dal Pozzo, Valentina, D’Arcangelo, Gabriella
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Society for Neuroscience 2015
Materias:
New Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4676199/
https://www.ncbi.nlm.nih.gov/pubmed/26693177
http://dx.doi.org/10.1523/ENEURO.0046-15.2015

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4676199/
https://www.ncbi.nlm.nih.gov/pubmed/26693177
http://dx.doi.org/10.1523/ENEURO.0046-15.2015

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