Heterozygous CAPZA2 mutations cause global developmental delay, hypotonia with epilepsy: a case report and the literature review-Reference-Cited by-同舟云学术

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Heterozygous CAPZA2 mutations cause global developmental delay, hypotonia with epilepsy: a case report and the literature review

Published:2024-02-19 Issue:5 Volume:69 Page:197-203
ISSN:1434-5161
Container-title:Journal of Human Genetics
language:en
Short-container-title:J Hum Genet

Author:

Zhang Xiao-Man,Xu Kai-Li,Kong Jing-Hui,Dong Geng,Dong Shi-Jie,Yang Zhi-Xiao,Xu Shu-Jing,Wang Li,Luo Shu-Ying,Zhang Yao-Dong,Zhou Chong-Chen,Gu Wei-Yue,Mei Shi-Yue

Publisher

Springer Science and Business Media LLC

Link

https://www.nature.com/articles/s10038-024-01230-z.pdf

Reference25 articles.

1. Bastos F, Cross JH. Epilepsy. Handb Clin Neurol. 2020;174:137–58.

2. Guerrini R. Epilepsy in children. Lancet. 2006;367:499–524.

3. Fine A, Wirrell EC. Seizures in Children. Pediatr Rev. 2020;41:321–47.

4. Carney P, Prowse MA, Scheffer IE. Epilepsy syndromes in children. Aust Fam Physician. 2005;34:1009–15.

5. Sharma P, Hussain A, Greenwood R. Precision in pediatric epilepsy. F1000Res. 2019;8:F1000.

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