Clinical and pathological features in adult-onset NIID patients with cortical enhancement

Author:

Liang Huiting,Wang Bo,Li Qing,Deng Jianwen,Wang Lulu,Wang Huan,Li Xiaobin,Zhu Min,Cai Yu,Wang Zhaoxia,Yuan Yun,Fang Pu,Hong DaojunORCID

Funder

National Natural Science Foundation of China

Recruitment Program of Global Experts

Publisher

Springer Science and Business Media LLC

Subject

Clinical Neurology,Neurology

Reference26 articles.

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2. Wang Y, Wang B, Wang L, Yao S, Zhao J, Zhong S, Cong L, Liu L, Zhang J, Zhang J, Hong D (2020) Diagnostic indicators for adult-onset neuronal intranuclear inclusion disease. Clin Neuropathol 39(1):7–18. https://doi.org/10.5414/NP301203

3. Deng J, Gu M, Miao Y, Yao S, Zhu M, Fang P, Yu X, Li P, Su Y, Huang J, Zhang J, Yu J, Li F, Bai J, Sun W, Huang Y, Yuan Y, Hong D, Wang Z (2019) Long-read sequencing identified repeat expansions in the 5'UTR of the NOTCH2NLC gene from Chinese patients with neuronal intranuclear inclusion disease. J Med Genet 56(11):758–764. https://doi.org/10.1136/jmedgenet-2019-106268

4. Tian Y, Wang JL, Huang W, Zeng S, Jiao B, Liu Z, Chen Z, Li Y, Wang Y, Min HX, Wang XJ, You Y, Zhang RX, Chen XY, Yi F, Zhou YF, Long HY, Zhou CJ, Hou X, Wang JP, Xie B, Liang F, Yang ZY, Sun QY, Allen EG, Shafik AM, Kong HE, Guo JF, Yan XX, Hu ZM, Xia K, Jiang H, Xu HW, Duan RH, Jin P, Tang BS, Shen L (2019) Expansion of human-specific GGC repeat in neuronal intranuclear inclusion disease-related disorders. Am J Hum Genet 105(1):166–176. https://doi.org/10.1016/j.ajhg.2019.05.013

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