De Novo and Inherited SETD1A Variants in Early-onset Epilepsy-Reference-Cited by-同舟云学术

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De Novo and Inherited SETD1A Variants in Early-onset Epilepsy

Published:2019-06-13 Issue:6 Volume:35 Page:1045-1057
ISSN:1673-7067
Container-title:Neuroscience Bulletin
language:en
Short-container-title:Neurosci. Bull.

Author:

Yu Xiuya,Yang Lin,Li Jin,Li Wanxing,Li Dongzhi,Wang Ran,Wu Kai,Chen Wenhao,Zhang Yi,Qiu Zilong,Zhou Wenhao

Publisher

Springer Science and Business Media LLC

Subject

General Medicine,Physiology,General Neuroscience

Link

http://link.springer.com/content/pdf/10.1007/s12264-019-00400-w.pdf

Reference26 articles.

1. Eltze CM, Chong WK, Cox T, Whitney A, Cortina-Borja M, Chin RF, et al. A population-based study of newly diagnosed epilepsy in infants. Epilepsia 2013, 54: 437–445.

2. Hauser WA, Kurland LT. The epidemiology of epilepsy in Rochester, Minnesota, 1935 through 1967. Epilepsia 1975, 16: 1–66.

3. Deprez L, Jansen A, De Jonghe P. Genetics of epilepsy syndromes starting in the first year of life. Neurology 2009, 72: 273–281.

4. Picco G, Garnett MJ. A road map for precision cancer medicine using personalized models. Cancer Discov 2017, 7: 456–458.

5. Lee EH. Epilepsy syndromes during the first year of life and the usefulness of an epilepsy gene panel. Korean J Pediatr 2018, 61: 101–107.

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