Reversal of learning deficits in a Tsc2(+/−) mouse model of tuberous sclerosis

Tuberous sclerosis is a single-gene disorder caused by heterozygous mutations in the TSC1 (9q34) or TSC2 (16p13.3) gene1,2 and is frequently associated with mental retardation, autism and epilepsy. Even individuals with tuberous sclerosis and a normal intelligence quotient (approximately 50%)3–5 are...

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Detaylı Bibliyografya
Asıl Yazarlar: Ehninger, Dan, Han, Sangyeul, Shilyansky, Carrie, Zhou, Yu, Li, Weidong, Kwiatkowski, David J, Ramesh, Vijaya, Silva, Alcino J
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 2008
Konular:
Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC2664098/
https://ncbi.nlm.nih.gov/pubmed/18568033
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/nm1788
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