Genetic analysis of benign familial epilepsies in the first year of life in a Chinese cohort-Reference-Cited by-同舟云学术

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Genetic analysis of benign familial epilepsies in the first year of life in a Chinese cohort

Published:2017-11-13 Issue:1 Volume:63 Page:9-18
ISSN:1434-5161
Container-title:Journal of Human Genetics
language:en
Short-container-title:J Hum Genet

Author:

Zeng Qi,Yang Xiaoling,Zhang Jing,Liu Aijie,Yang Zhixian,Liu Xiaoyan,Wu Ye,Wu Xiru,Wei Liping,Zhang Yuehua

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

https://www.nature.com/articles/s10038-017-0359-x.pdf

Reference35 articles.

1. Vigevano F, Fusco L, Di Capua M, Ricci S, Sebastianelli R, Lucchini P. Benign infantile familial convulsions. Eur J Pediatr. 1992;151:608–12.

2. Okumura A, Hayakawa F, Kato T, Kuno K, Negoro T, Watanabe K. Early recognition of benign partial epilepsy in infancy. Epilepsia. 2000;41:714–7.

3. Tomlinson SE, Bostock H, Grinton B, Hanna MG, Kullmann DM, Kiernan MC, et al. In vivo loss of slow potassium channel activity in individuals with benign familial neonatal epilepsy in remission. Brain. 2012;135:3144–52.

4. Kaplan RE, Lacey DJ. Benign familial neonatal-infantile seizures. Am J Med Genet. 1983;16:595–9.

5. Vigevano F. Benign familial infantile seizures. Brain Dev. 2005;27:172–7.

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