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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...

पूर्ण विवरण

में बचाया:
ग्रंथसूची विवरण
में प्रकाशित:Sci Rep
मुख्य लेखकों: 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.
स्वरूप: Artigo
भाषा:Inglês
प्रकाशित: Nature Publishing Group UK 2018
विषय:
ऑनलाइन पहुंच: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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