Brain Proteomic Profiling in Intractable Epilepsy Caused by TSC1 Truncating Mutations: A Small Sample Study

Brain Proteomic Profiling in Intractable Epilepsy Caused by TSC1 Truncating Mutations: A Small Sample Study

Tuberous sclerosis complex (TSC) is a genetic disease characterized by seizures, mental deficiency, and abnormalities of the skin, brain, kidney, heart, and lungs. TSC is inherited in an autosomal dominant manner and is caused by variations in either the TSC1 or TSC2 gene. TSC-related epilepsy (TRE)...

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Bibliographic Details
Main Authors: Yi-Dan Liu, Meng-Yu Ma, Xi-Bin Hu, Huan Yan, Yan-Ke Zhang, Hao-Xiang Yang, Jing-Hui Feng, Lin Wang, Hao Zhang, Bin Zhang, Qiu-Bo Li, Jun-Chen Zhang, Qing-Xia Kong
Format: Article
Language:English
Published: Frontiers Media S.A. 2020-05-01
Series:Frontiers in Neurology
Subjects:
tuberous sclerosis complex
TSC1 gene
epilepsy
proteomic profiling
mutation
Online Access:https://www.frontiersin.org/article/10.3389/fneur.2020.00475/full

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https://www.frontiersin.org/article/10.3389/fneur.2020.00475/full

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